Standard Practices for Bulk Sample Collection and Swab Sample Collection of Visible Powders Suspected of Being Biological Agents and Toxins from Nonporous Surfaces

SIGNIFICANCE AND USE
4.1 These practices should be used only to collect visible samples that are suspected biological agents and toxins and have been field screened as defined by the FBI-DHS-HHS/CDC Coordinated Document for explosive hazard, radiological hazard, and other acute chemical hazards.  
4.2 These practices provide standardized methods for collecting, packaging, and transporting suspicious visible powder samples that are suspected biological agents and toxins. Collection of a bulk powder material from a nonporous surface using a sterile swab and laminated card as the collection devices to move the material into a container will depend on several factors, including (but not limited to): (1) amount of visible powder present; (2) sample composition; (3) choice of collection device; (4) size and shape of the collection container; (5) ability of the powder to become aerosolized; (6) texture and porosity of the surface;  (7) humidity; (8) air movement; and (9) electrostatic properties of powders and collection tools/containers.  
4.3 Similarly, these practices standardize methods for sampling suspicious visible powders for on-site analysis, although wipe and swab sampling is often employed in the field for subsequent LRN reference laboratory analysis. The ability to collect suitable samples from nonporous surfaces using a sterile moistened swab will depend on the following factors: (1) swabbing procedure;  (2) swab material; (3) sample composition; and (4) texture of the surface.  
4.4 These practices standardize suspicious powder collection and packaging procedures and swab sampling procedures in order to reduce exposure risk, to reduce variability associated with sample handling and sample analysis, and to increase reliability of sampling visible powder samples from nonporous surfaces.  
4.5 The bulk sample collection practice and the swab sampling practice are recommended for collecting amassed or dispersed powder samples from all nonporous surfaces on which the suspicious po...
SCOPE
1.1 These practices address collection of visible powders that are suspected biological agents and toxins from solid nonporous surfaces using a bulk collection method, using a dry swab and laminated card, followed by a swab sampling method using a sterile moistened swab. Bulk powder samples are collected and packaged in a manner that permits the maximum amount of the sample to be safely transported to a reference laboratory within the Centers for Disease Control and Prevention (CDC) national Laboratory Response Network (LRN)2 for confirmatory identification and safe storage. If the source of the powder is a letter or small package, that item is also packaged in a manner that permits it to be safely transported to an LRN reference laboratory. A sterile moistened swab may be used to collect residual powder from the nonporous surface and may be used to conduct on-site biological assessments for the purpose of testing for biological agents and toxins.  
1.2 These practices are performed in coordination with the Federal Bureau of Investigation (FBI) as part of a risk assessment including hazard assessment and threat credibility evaluation as recommended and clarified in Guide E2770. The decision to implement these practices and collect a public safety sample will be made by members of the response community of the jurisdiction assuming responsibility through coordination with the FBI and the receiving LRN reference laboratory.  
1.3 Sample Collection Method A covers the bulk collection and packaging of suspicious visible powders that are suspected biological agents and toxins from solid nonporous surfaces. All samples suspected to be biological agents and toxins on nonporous surfaces should be collected according to Sample Collection Method A and sent to an LRN reference laboratory for confirmatory testing.  
1.4 Sample Collection Method B covers swab sampling of residual suspicious powders that are suspected biological ag...

General Information

Status
Published
Publication Date
14-May-2017

Relations

Effective Date
15-May-2017
Effective Date
01-Aug-2018
Effective Date
01-Aug-2018
Effective Date
01-Feb-2018
Effective Date
01-Nov-2017
Effective Date
01-Apr-2017
Effective Date
01-Jul-2011
Effective Date
01-Jul-2011
Effective Date
01-Mar-2005
Effective Date
01-Mar-2005
Effective Date
15-May-2017
Effective Date
15-May-2017
Effective Date
15-May-2017
Effective Date
15-May-2017
Effective Date
15-May-2017

Overview

ASTM E2458-17 provides standard practices for the collection and handling of visible powder samples that are suspected of being biological agents and toxins from nonporous surfaces. Developed by ASTM International, this standard establishes consistent procedures for safely collecting, packaging, and transporting bulk powder and swab samples to accredited laboratories for confirmatory identification. These practices are designed to support emergency response operations, reduce exposure risk, ensure the integrity of forensic evidence, and enhance the reliability of biological threat sampling.

Key Topics

  • Sample Collection Methods: The standard details two primary collection methods:
    • Bulk Collection (Method A): Gathering and packaging visible powder samples using sterile swabs and laminated cards.
    • Swab Sampling (Method B): Collecting residual powders from nonporous surfaces for optional on-site biological assessments.
  • Field Screening: Prior to sample collection, visible powders must undergo field screening to assess for explosive, radiological, and acute chemical hazards, following FBI-DHS-HHS/CDC guidelines.
  • Standardized Procedures: Outlines step-by-step processes for:
    • Selecting appropriate collection devices and containers
    • Labeling and documentation
    • Chain of custody requirements
    • Appropriate use of personal protective equipment (PPE)
    • Minimizing contamination and sample loss during collection and transport
  • Coordination and Compliance: Practices are to be performed in cooperation with the FBI, LRN laboratories, and other relevant authorities, ensuring regulatory and biosecurity compliance.
  • Limitations: These practices are intended for visible powders on solid nonporous surfaces; not recommended for porous materials such as fabrics or carpets.

Applications

ASTM E2458-17 is highly relevant for first responders, public health officials, hazardous materials (HAZMAT) teams, and forensic laboratory personnel involved in the emergency response to biological threats or suspicious powders. Practical uses include:

  • Law Enforcement and Public Safety: Supporting risk assessment, evidence preservation, and threat investigations through standardized biological sample collection from letters, packages, building surfaces, and equipment.
  • Biosafety and Hazard Mitigation: Minimizing the risk of exposure to potential biological agents and ensuring the safe handling and transport of samples to national Laboratory Response Network (LRN) reference laboratories.
  • Incident Response Planning: Providing guidelines for training, competency evaluation, and the coordination of multiple agencies during biological incident response.
  • Regulatory Compliance: Ensuring all sampling, packaging, transportation, and documentation activities meet federal regulations-including OSHA, EPA, DOT, and IATA standards.

Related Standards

Professionals applying ASTM E2458-17 may also reference related standards and guidance for comprehensive incident management:

  • ASTM E2770: Guide for operational guidelines for initial response to suspected biological agents and toxins.
  • NFPA 472: Standard for responder competence at hazardous materials incidents.
  • CDC/NIOSH Surface Sampling Procedures: For monitoring Bacillus anthracis spores.
  • DOT 49 CFR 171-180: Hazardous Materials Regulations for transportation.
  • IATA PI 602 & PI 650: Regulations for shipping infectious substances and diagnostic samples.
  • OSHA 29 CFR 1910.120: Standards for hazardous waste operations and emergency response.
  • FBI-DHS-HHS/CDC Coordinated Document: Guidance on field screening for biological, chemical, and radiological hazards.

Summary

ASTM E2458-17 plays a vital role in standardizing the collection and handling of visible powders suspected to be biological agents or toxins from nonporous surfaces. By following these best practices, organizations contribute to public safety, ensure the validity of forensic evidence, and reduce the risks associated with potential biothreat incidents. This standard is an essential resource for agencies responsible for homeland security, emergency management, and laboratory biosecurity.

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Frequently Asked Questions

ASTM E2458-17 is a standard published by ASTM International. Its full title is "Standard Practices for Bulk Sample Collection and Swab Sample Collection of Visible Powders Suspected of Being Biological Agents and Toxins from Nonporous Surfaces". This standard covers: SIGNIFICANCE AND USE 4.1 These practices should be used only to collect visible samples that are suspected biological agents and toxins and have been field screened as defined by the FBI-DHS-HHS/CDC Coordinated Document for explosive hazard, radiological hazard, and other acute chemical hazards. 4.2 These practices provide standardized methods for collecting, packaging, and transporting suspicious visible powder samples that are suspected biological agents and toxins. Collection of a bulk powder material from a nonporous surface using a sterile swab and laminated card as the collection devices to move the material into a container will depend on several factors, including (but not limited to): (1) amount of visible powder present; (2) sample composition; (3) choice of collection device; (4) size and shape of the collection container; (5) ability of the powder to become aerosolized; (6) texture and porosity of the surface; (7) humidity; (8) air movement; and (9) electrostatic properties of powders and collection tools/containers. 4.3 Similarly, these practices standardize methods for sampling suspicious visible powders for on-site analysis, although wipe and swab sampling is often employed in the field for subsequent LRN reference laboratory analysis. The ability to collect suitable samples from nonporous surfaces using a sterile moistened swab will depend on the following factors: (1) swabbing procedure; (2) swab material; (3) sample composition; and (4) texture of the surface. 4.4 These practices standardize suspicious powder collection and packaging procedures and swab sampling procedures in order to reduce exposure risk, to reduce variability associated with sample handling and sample analysis, and to increase reliability of sampling visible powder samples from nonporous surfaces. 4.5 The bulk sample collection practice and the swab sampling practice are recommended for collecting amassed or dispersed powder samples from all nonporous surfaces on which the suspicious po... SCOPE 1.1 These practices address collection of visible powders that are suspected biological agents and toxins from solid nonporous surfaces using a bulk collection method, using a dry swab and laminated card, followed by a swab sampling method using a sterile moistened swab. Bulk powder samples are collected and packaged in a manner that permits the maximum amount of the sample to be safely transported to a reference laboratory within the Centers for Disease Control and Prevention (CDC) national Laboratory Response Network (LRN)2 for confirmatory identification and safe storage. If the source of the powder is a letter or small package, that item is also packaged in a manner that permits it to be safely transported to an LRN reference laboratory. A sterile moistened swab may be used to collect residual powder from the nonporous surface and may be used to conduct on-site biological assessments for the purpose of testing for biological agents and toxins. 1.2 These practices are performed in coordination with the Federal Bureau of Investigation (FBI) as part of a risk assessment including hazard assessment and threat credibility evaluation as recommended and clarified in Guide E2770. The decision to implement these practices and collect a public safety sample will be made by members of the response community of the jurisdiction assuming responsibility through coordination with the FBI and the receiving LRN reference laboratory. 1.3 Sample Collection Method A covers the bulk collection and packaging of suspicious visible powders that are suspected biological agents and toxins from solid nonporous surfaces. All samples suspected to be biological agents and toxins on nonporous surfaces should be collected according to Sample Collection Method A and sent to an LRN reference laboratory for confirmatory testing. 1.4 Sample Collection Method B covers swab sampling of residual suspicious powders that are suspected biological ag...

SIGNIFICANCE AND USE 4.1 These practices should be used only to collect visible samples that are suspected biological agents and toxins and have been field screened as defined by the FBI-DHS-HHS/CDC Coordinated Document for explosive hazard, radiological hazard, and other acute chemical hazards. 4.2 These practices provide standardized methods for collecting, packaging, and transporting suspicious visible powder samples that are suspected biological agents and toxins. Collection of a bulk powder material from a nonporous surface using a sterile swab and laminated card as the collection devices to move the material into a container will depend on several factors, including (but not limited to): (1) amount of visible powder present; (2) sample composition; (3) choice of collection device; (4) size and shape of the collection container; (5) ability of the powder to become aerosolized; (6) texture and porosity of the surface; (7) humidity; (8) air movement; and (9) electrostatic properties of powders and collection tools/containers. 4.3 Similarly, these practices standardize methods for sampling suspicious visible powders for on-site analysis, although wipe and swab sampling is often employed in the field for subsequent LRN reference laboratory analysis. The ability to collect suitable samples from nonporous surfaces using a sterile moistened swab will depend on the following factors: (1) swabbing procedure; (2) swab material; (3) sample composition; and (4) texture of the surface. 4.4 These practices standardize suspicious powder collection and packaging procedures and swab sampling procedures in order to reduce exposure risk, to reduce variability associated with sample handling and sample analysis, and to increase reliability of sampling visible powder samples from nonporous surfaces. 4.5 The bulk sample collection practice and the swab sampling practice are recommended for collecting amassed or dispersed powder samples from all nonporous surfaces on which the suspicious po... SCOPE 1.1 These practices address collection of visible powders that are suspected biological agents and toxins from solid nonporous surfaces using a bulk collection method, using a dry swab and laminated card, followed by a swab sampling method using a sterile moistened swab. Bulk powder samples are collected and packaged in a manner that permits the maximum amount of the sample to be safely transported to a reference laboratory within the Centers for Disease Control and Prevention (CDC) national Laboratory Response Network (LRN)2 for confirmatory identification and safe storage. If the source of the powder is a letter or small package, that item is also packaged in a manner that permits it to be safely transported to an LRN reference laboratory. A sterile moistened swab may be used to collect residual powder from the nonporous surface and may be used to conduct on-site biological assessments for the purpose of testing for biological agents and toxins. 1.2 These practices are performed in coordination with the Federal Bureau of Investigation (FBI) as part of a risk assessment including hazard assessment and threat credibility evaluation as recommended and clarified in Guide E2770. The decision to implement these practices and collect a public safety sample will be made by members of the response community of the jurisdiction assuming responsibility through coordination with the FBI and the receiving LRN reference laboratory. 1.3 Sample Collection Method A covers the bulk collection and packaging of suspicious visible powders that are suspected biological agents and toxins from solid nonporous surfaces. All samples suspected to be biological agents and toxins on nonporous surfaces should be collected according to Sample Collection Method A and sent to an LRN reference laboratory for confirmatory testing. 1.4 Sample Collection Method B covers swab sampling of residual suspicious powders that are suspected biological ag...

ASTM E2458-17 is classified under the following ICS (International Classification for Standards) categories: 13.300 - Protection against dangerous goods; 71.040.40 - Chemical analysis; 87.040 - Paints and varnishes. The ICS classification helps identify the subject area and facilitates finding related standards.

ASTM E2458-17 has the following relationships with other standards: It is inter standard links to ASTM E2458-10, ASTM F2413-18, ASTM F2412-18a, ASTM F2412-18, ASTM F2413-17, ASTM E2770-17, ASTM F2412-11, ASTM F2413-11, ASTM F2412-05, ASTM F2413-05, ASTM E3095-17, ASTM E2771-11(2019), ASTM E2805-18, ASTM E2800-11(2017), ASTM E2852-13(2021). Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

ASTM E2458-17 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.

Standards Content (Sample)


This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the
Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Designation: E2458 − 17
Standard Practices for
Bulk Sample Collection and Swab Sample Collection of
Visible Powders Suspected of Being Biological Agents and
Toxins from Nonporous Surfaces
This standard is issued under the fixed designation E2458; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope Collection Method A and sent to an LRN reference laboratory
for confirmatory testing.
1.1 These practices address collection of visible powders
that are suspected biological agents and toxins from solid 1.4 Sample Collection Method B covers swab sampling of
nonporoussurfacesusingabulkcollectionmethod,usingadry residual suspicious powders that are suspected biological
swabandlaminatedcard,followedbyaswabsamplingmethod agents and toxins from solid nonporous surfaces. Swab
using a sterile moistened swab. Bulk powder samples are samplescanbeusedforon-sitebiologicalassessment;however
collected and packaged in a manner that permits the maximum results from on-site biological assessments are not definitive;
amount of the sample to be safely transported to a reference confirmatory testing by the LRN reference laboratory is
laboratory within the Centers for Disease Control and Preven- necessary to make public health decisions.
tion (CDC) national Laboratory Response Network (LRN) for
1.5 These practices incorporate reference guidance for
confirmatoryidentificationandsafestorage.Ifthesourceofthe
packaging and transport of suspicious visible powders to
powder is a letter or small package, that item is also packaged
comply with all appropriate federal regulations regarding
in a manner that permits it to be safely transported to an LRN
biosafety and biosecurity.
reference laboratory. A sterile moistened swab may be used to
1.6 These practices should only be used to collect visible
collectresidualpowderfromthenonporoussurfaceandmaybe
samples that are suspected biological agents and toxins and
used to conduct on-site biological assessments for the purpose
have been field screened according to reference guidance for
of testing for biological agents and toxins.
explosivehazard,radiologicalhazard,andotheracutechemical
1.2 These practices are performed in coordination with the
hazards.
Federal Bureau of Investigation (FBI) as part of a risk
1.7 The values stated in SI units are to be regarded as
assessment including hazard assessment and threat credibility
standard. The values given in parentheses are for information
evaluation as recommended and clarified in Guide E2770. The
only.
decision to implement these practices and collect a public
safety sample will be made by members of the response 1.8 This standard does not purport to address all of the
safety concerns associated with its use. It is the responsibility
community of the jurisdiction assuming responsibility through
coordination with the FBI and the receiving LRN reference of the user of this standard to establish appropriate safety and
health practices and determine the applicability of regulatory
laboratory.
limitations prior to use.
1.3 Sample Collection MethodAcovers the bulk collection
1.9 This international standard was developed in accor-
and packaging of suspicious visible powders that are suspected
dance with internationally recognized principles on standard-
biologicalagentsandtoxinsfromsolidnonporoussurfaces.All
ization established in the Decision on Principles for the
samples suspected to be biological agents and toxins on
Development of International Standards, Guides and Recom-
nonporous surfaces should be collected according to Sample
mendations issued by the World Trade Organization Technical
Barriers to Trade (TBT) Committee.
These practices are under the jurisdiction of ASTM Committee E54 on
2. Referenced Documents
Homeland Security Applications and are the direct responsibility of Subcommittee
2.1 ASTM Standards:
E54.01 on CBRNE Sensors and Detectors.
Current edition approved May 15, 2017. Published June 2017. Originally
approved in 2006. Last previous edition approved in 2010 as E2458 – 10. DOI:
10.1520/E2458-17. For referenced ASTM standards, visit the ASTM website, www.astm.org, or
The CDC Laboratory Response Network is the network responsible for contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM
handling clinical specimens and environmental samples containing suspected Standards volume information, refer to the standard’s Document Summary page on
biothreat agents. the ASTM website.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
E2458 − 17
E2770 GuideforOperationalGuidelinesforInitialResponse 2.4 NFPA Standards:
to Suspected Biological Agents and Toxins NFPA 472 Standard for Competence of Responders to Haz-
ardous Materials/Weapons of Mass Destruction Incidents,
F2412 Test Methods for Foot Protection
2013 Edition
F2413 Specification for Performance Requirements for Pro-
NFPA1994 StandardonProtectiveEnsemblesforChemical/
tective (Safety) Toe Cap Footwear
Biological Terrorism Incidents
2.2 Federal Government Regulations:
2.5 IATA Standards:
18 USC 178 Prohibitions with respect to biological weapons
IATA PI 602 Infectious Diseases (Infectious Substances)
DOT 49 CFR, Parts 171-180 Hazardous Materials Regula-
IATA PI 650 Shipping of Diagnostic Samples
tions
IATA DGR 46th Edition, 2005
DOT - 49 CFR 172 Subpart H, Transportation Training
IATA DGR Addendum I, January 2005
DOT - 49 CFR 173 General Requirements for Shipments
IATA DGR Addendum II, March 2005
and Packagings
IATA DGR Addendum III, July 2005
DOT - 49 CFR 178 Specifications for Packagings
2.6 ANSI Standards:
EPA - 40 CFR 300 National Oil and Hazardous Substances
ANSI Z41-1999 American National Standard for Personal
Pollution Contingency Plan (NCP)
Protection - Protective Footwear
EPA - 40 CFR 311 Worker Protection
ANSI Z87.1-2003 American National Standard for Occupa-
NRC-10CFR20 StandardsforProtectionagainstRadiation
tional and Educational Personal Eye and Face Protection
NIOSH - 42 CFR 84 Respiratory Protective Devices
Devices
OSHA- 29 CFR 1910 Subpart Z and 29 CFR 1926 Subpart
ANSI Z88.2-1992 American National Standard Practices for
Z Toxic and Hazardous Substances
Respiratory Protection
OSHA- 29 1910.1096 and 29 CFR 1926.53 Ionizing Radia- ANSI Z88.10-2001 American National Standard for Per-
tion sonal Protection - Respirator Fit Testing Methods
ANSI/ISEA Z89.1-2003 American National Standard for
OSHA- 29 CFR 1910.120 Hazardous Waste Operations and
Personal Protection - Protective Headwear for Industrial
Emergency Response (HAZWOPER) standard
Workers Requirements
OSHA - 29 CFR 1910 Subpart I (Sections 132 to 139) Per-
ANSI/Compressed GasAssociation, CGAG-7.1-1997 Com-
sonal Protective Equipment
modity Specification for Air
OSHA - 29 CFR 1910.1200 Hazard Communication
2.7 IAFC Guidance:
2.3 Federal Guidance:
Model Procedures for Responding to a Package with Sus-
OSHA - CPL 02-02-073 Inspection Procedures for 29 CFR
picion of a Biological Threat, October 2008
1910.120 and 1926.65, Paragraph (q): Emergency Re-
sponse to Hazardous Substance Releases
3. Terminology
NIOSH Publication No. 2009-132 Recommendations for the
3.1 Definitions:
Selection and Use of Respirators and Protective Clothing
3.1.1 aseptic technique, n—operation or performance of a
for Protection Against Biological Agents
procedure or method under carefully controlled conditions to
FBI Laboratory Publication Handbook of Forensic Services
reduce the risk of exposure and prevent the introduction of
unwanted material/matter (contamination) into a sample.
FBI-DHS-HHS/CDC Coordinated Document Guidance on
3.1.2 biological agent, n—any microorganism (including
Initial Response to a Suspicious Letter/Container with a
but not limited to, bacteria, viruses, fungi, rickettsiae, or
Potential Biological threat, November 2, 2004
protozoa), or infectious substance, or any naturally occuring,
CDC/NIOSH Surface Sampling Procedures for Bacillus an-
bioengineered or synthesized component of any such microor-
thracis Spores from Smooth, Non-porous Surfaces, April
ganism or infectious substance, capable of causing: (1) death,
26, 2012
disease or other biological malfunction in a human, an animal,
DHS Framework for a Biothreat Field Response Mission
a plant, or another living organism; (2) deterioration of food,
Capability, April 2011
water, equipment, supplies, or material of any kind; or (3)
Sandia National Laboratories SAND2005-3237 (LBNL-
deleterious alteration of the environment. 18 USC 178
54973 (II)) Guidelines to Improve Airport Preparedness
3.1.3 bulk powder, n—a visible powder, at least approxi-
Against Chemical and Biological Terrorism
mately5mL(1teaspoon)involumeamassedordispersedover
4 8
AvailablefromU.S.GovernmentPrintingOfficeSuperintendentofDocuments, Available from National Fire Protection Association (NFPA), 1 Batterymarch
732N.CapitolSt.,NW,MailStop:SDE,Washington,DC20401,andalsoavailable Park, Quincy, MA 02269-9101.
online from Occupational Safety and Health Administration (www.osha.gov). Available from the InternationalAir TransportAssociation, 800 Place Victoria,
Available from http://www.cdc.gov/niosh/topics/emres/surface-sampling- PO Box 113, Montreal-H4Z 1M1, Quebec, Canada.
bacillus-anthracis.html. Available fromAmerican National Standards Institute (ANSI), 25W. 43rd St.,
Available from http://www.hsdl.org/?view&did=767721. 4th Floor, New York, NY 10036, http://www.ansi.org.
7 11
Available from http://share-ng.sandia.gov/news/resources/releases/2005/ Available from International Association of Fire Chiefs (IAFC), 4025 Fair
images/unlsand-2005-3237.pdf. Ridge Drive, Suite 300 Fairfax, VA 22033, http://www.iafc.org.
E2458 − 17
a limited area (optimally, area should be less than 20 by 20 cm 3.1.15 risk, n—the probability of suffering a loss or harm or
(approximately 8 by 8 in.). injury; peril.
3.1.16 toxin, n—the toxic material or product of plants,
3.1.4 chain of custody, n—set of procedures and documents
animals, microorganisms (including but not limited to,
to account for the integrity of sample by tracking its handling
bacteria, viruses, fungi, rickettsiae, or protozoa), or infectious
and storage from point of sample collection to final disposition
substances, or a recombinant or synthesized molecule, what-
of the sample.
ever their origin and method of production, and includes: (1)
3.1.5 cold zone, n—the uncontaminated area where workers
any poisonous substance or biological product that may be
are unlikely to be exposed to hazardous substances or danger-
engineered as a result of biotechnology produced by a living
ous conditions; also known as Clean Zone or Support Zone.
organism; or (2) any poisonous isomer or biological product,
CPL 02-02-071 Directive
homolog, or derivative of such a substance (18 USC 178).
3.1.6 confirmatory analysis, n—a test or a series of assays
3.1.17 threat, n—an indication of possible violence, harm,
that definitively identifies the presence of a suspected sub-
or danger and may include an indication of intent and
stance or agent.
capability. NIMS
3.1.6.1 Discussion—Confirmatory analysis of a biological
3.1.18 warm zone, n—the transition area between the Ex-
agent for public health action can be performed only by an
clusion Zone (ExZ or hot zone) and the Support Zone (SZ or
LRN national or reference laboratory.
cold zone) used to reduce and limit the amount of contamina-
3.1.7 decontamination,n—thephysicalorchemicalprocess,
tion on people and equipment, and in the air, water, and soil
or both, of reducing and preventing the spread of contaminants
that may be transferred into nonhazardous areas; the CRZ
from people, animals, the environment, or equipment involved
contains decontamination facilities, and functions as a buffer
at hazardous materials/weapons of mass destruction (WMD)
zone surrounding the ExZ; also known as the contamination
incidents. NFPA
reduction zone or CRZ. CPL 02-02-071 Directive
3.1.8 field screening, n—field measurements utilized early
3.1.19 weapon of mass destruction (WMD), n—any weapon
in the response to define and characterize the potential hazards
or device that is intended, or has the capability, to cause death
present, including corrosive, flammable, volatile, radioactive,
or serious bodily injury to a significant number of people
or oxidizer hazards, and to support tactical decision making to
through the release, dissemination, or impact of (1) toxic or
address operational safety measures.
poisonous chemicals or their precursors; (2) a disease organ-
ism; or (3) radiation or radioactivity. U.S. Code Title 50, Ch.
3.1.8.1 Discussion—Field screening does not include mea-
surements of biological properties, which is termed on-site 40, Sect. 2302, War and National Defense Definitions
biological assessments (see 3.1.12).
3.2 Acronyms:
3.2.1 AHJ—Authority Having Jurisdiction
3.1.9 hazard, n—something that is potentially dangerous or
harmful, often the root cause of an unwanted outcome; a
3.2.2 ANSI—American National Standards Institute
danger or peril. NIMS
3.2.3 ASTM—American Society for Testing and Materials
3.1.10 hot zone, n—the area, located on the site where
3.2.4 CDC—Centers for Disease Control and Prevention
contamination is either known or expected and where potential
3.2.5 CFR—Code of Federal Regulations
for greatest exposure exists; also known as Exclusion Zone or
ExZ. CPL 02-02-071 Directive
3.2.6 CRZ—Contamination Reduction Zone
3.1.11 incident commander (IC), n—the individual respon- 3.2.7 CST—Civil Support Team
sible for all incident activities, including the development of
3.2.8 DHS—Department of Homeland Security
strategies and tactics and the ordering and release of resources.
3.2.9 DOT—Department of Transportation
3.1.11.1 Discussion—The IC has overall authority and re-
3.2.10 EOC—Emergency Operations Center
sponsibility for conducting incident operations and is respon-
sible for the management of all incident operations at the
3.2.11 EPA—Environmental Protection Agency
incident site. NIMS
3.2.12 ExZ—Exclusion Zone
3.1.12 on-site biological assessment, n—measurements of
3.2.13 FBI—Federal Bureau of Investigation
properties inherent to biological materials performed in the
3.2.14 FEMA—Federal Emergency Management Agency
field using rapid, field-based procedures and assays.
3.2.15 HAZMAT—Hazardous Materials
3.1.13 personal protective equipment (PPE), n—equipment
3.2.16 HHS—Health and Human Services
provided to shield or isolate a person from the chemical,
biological, physical, and thermal hazards that can be encoun-
3.2.17 IAFC—International Association of Fire Chiefs
tered at hazardous materials/weapons of mass destruction
3.2.18 IATA—International Air Transport Association
(WMD) incidents. NFPA
3.2.19 IC—Incident Commander
3.1.14 presumptive test, n—non-definitive test used to
3.2.20 ICS—Incident Command System
evaluate a material for the presence of a substance or agent, or
the presence of signatures of a substance or agent. 3.2.21 IEC—International Electrotechnical Commission
E2458 − 17
3.2.22 ISEA—International Safety Equipment Association 4.6 These practices are not recommended for samples on
porous materials such as upholstery, carpeting, air filters, or
3.2.23 ISO—International Organization for Standardization
ceiling tiles.
3.2.24 LRN—Laboratory Response Network
4.7 These practices are recommended for collecting visible
3.2.25 MACS—Multiagency Coordination System
powders where the bulk of the powder sample is amassed or
3.2.26 NFPA—National Fire Protection Association
dispersed over a limited area (optimally, area should be less
3.2.27 NIMS—National Incident Management System
than 20 by 20 cm (approximately 8 by 8 in.) or 400 cm
(approximately 64 in. ).
3.2.28 NIOSH—National Institute for Occupational Safety
and Health
4.8 These practices are to be performed by personnel who
3.2.29 NRC—Nuclear Regulatory Commission
are adequately trained to work with hazardous materials in the
hot zone (see NFPA 472, or OSHA - 29 CFR 1910.120).
3.2.30 OSHA—Occupational Safety and HealthAdministra-
Personnel performing collection or screening under these
tion
practices shall be adequately trained in the use of sampling
3.2.31 PBS—Phosphate Buffered Saline
equipment, materials, and procedures. This includes personnel
3.2.32 PPE—Personal Protective Equipment
performing the prior initial chemical and radiological screen-
3.2.33 SZ—Support Zone
ing. Personnel should use the appropriate level of personal
protective equipment (PPE) to mitigate hazards during collec-
3.2.34 US&R—Urban Search and Rescue
tion and screening. Personnel performing collection or screen-
3.2.35 WMD—Weapons of Mass Destruction
ing under these practices shall be aware of evidence preserva-
tion and sampling procedures (NFPA 472 section 6.5).
4. Significance and Use
4.1 These practices should be used only to collect visible
4.9 These standard practices should be used in accordance
samples that are suspected biological agents and toxins and
with Guide E2770 for best practices for planning, training and
have been field screened as defined by the FBI-DHS-HHS/
evaluation of competency.
CDCCoordinatedDocumentforexplosivehazard,radiological
SAMPLE COLLECTION METHOD A—BULK
hazard, and other acute chemical hazards.
SAMPLE COLLECTION FOR LABORATORY
4.2 These practices provide standardized methods for
ANALYSIS
collecting, packaging, and transporting suspicious visible pow-
der samples that are suspected biological agents and toxins.
5. Scope of Method A
Collection of a bulk powder material from a nonporous surface
5.1 This sample collection method applies to the bulk
using a sterile swab and laminated card as the collection
devices to move the material into a container will depend on collectionandpackagingofsuspiciousvisiblepowdersthatare
suspected biological agents or toxins, or both, from solid
several factors, including (but not limited to): (1) amount of
visible powder present; (2) sample composition; (3) choice of nonporous surfaces.
collection device; (4) size and shape of the collection con-
5.2 These practices are performed in coordination with the
tainer; (5) ability of the powder to become aerosolized; (6)
FBI and receiving LRN reference laboratory after a risk
texture and porosity of the surface; (7) humidity; (8) air
assessmentincludingahazardassessmentandthreatcredibility
movement; and (9) electrostatic properties of powders and
evaluation is conducted and the sample is deemed potentially
collection tools/containers.
to be a credible threat as recommended and clarified in Guide
4.3 Similarly, these practices standardize methods for sam-
E2770.
pling suspicious visible powders for on-site analysis, although
5.3 This sample collection method applies to suspicious
wipe and swab sampling is often employed in the field for
visible powders that are amassed or dispersed in a limited area
subsequent LRN reference laboratory analysis. The ability to
where the bulk of the powder sample is in an area that is less
collect suitable samples from nonporous surfaces using a
than 20 by 20 cm (approximately 8 by 8 in.) or 400 cm
sterile moistened swab will depend on the following factors:
(approximately 64 in. ).
(1) swabbing procedure; (2) swab material; (3) sample com-
position; and (4) texture of the surface.
5.4 These practices should be used only to collect samples
that are suspected biological agent and toxin hazards that have
4.4 These practices standardize suspicious powder collec-
been field screened as defined by the FBI-DHS-HHS/CDC
tion and packaging procedures and swab sampling procedures
Coordinated Document for explosive, radiological, and chemi-
in order to reduce exposure risk, to reduce variability associ-
cal hazards.
atedwithsamplehandlingandsampleanalysis,andtoincrease
reliability of sampling visible powder samples from nonporous
6. Summary of Sample Collection Method A
surfaces.
4.5 The bulk sample collection practice and the swab 6.1 A visible powder sample that is a suspected biological
sampling practice are recommended for collecting amassed or agent or toxin, or both, and its source should be field screened
dispersed powder samples from all nonporous surfaces on for non-biological hazards as defined in the FBI-DHS-HHS/
which the suspicious powder sample is clearly visible. CDC Coordinated Document and according to the reference
E2458 − 17
guidance including appropriate NFPA documents. Non- 7.12 Bucket, or other container marked “BIOHAZARD
biological hazards include explosive, radiological, and chemi- WASTE”.
cal hazards. The visible powder sample, amassed or dispersed
7.13 1-gal Sealable Plastic Bag(s), pre-labeled as “BIO-
in a limited area, is collected from a nonporous surface using
HAZARD WASTE”.
a swab and a laminated card to move the sample into a sterile
7.14 FieldScreeningResultsForm—SeeexampleinAppen-
dry collection container that is held close to the surface.
dix X1.
6.2 The method provides guidance on performing these
7.15 Sample Collection Sheet—See example in Appendix
procedures in a manner that will minimize sample loss and
X1. Note that a single sample collection sheet can be used for
aerosolization of the powder. The bulk powder sample and
all items collected at a single location including primary
swab are sent to an LRN reference laboratory for confirmatory
source, swab, and powder sample(s).
analysis.
7.16 Chain-of-Custody Form—See example in Appendix
7. Sampling and Packaging Equipment and Supplies
X1.
7.1 Personal Protective Equipment—Level A, B, or C
7.17 Two Plastic Transparent Document Pouches, with
personal protective equipment ensembles as indicated (see
adhesive on back.
Section 2 for additional guidance, including OSHA - 29 CFR
7.18 Durable Hard-sided Outer Container,withlidorscrew
1910.120 Appendix B and NFPA 1994).
cap, for sample transport (such as metal can with lid, or plastic
7.2 Clean drop cloth to create an isolated work area.
container with lid).
7.3 Sample Transport Container—Bucket or large heavy
7.19 Attach documentation described in the Sample Collec-
duty plastic bag used to transport the samples and materials
tion and Submission section of Guide E2770. Documentation
from the hot zone through to the decontamination line.
should include the contact information for local, state, and
federal law enforcement, local health officials and local/
7.4 Non-powdered Nitrile or Vinyl Examination Gloves.
national testing facilities.
7.5 Two Sterile Polypropylene Wide-mouth Screw-capped
Sample Collection Containers (Sample Containers)—
8. Procedure
Containers must possess a leak-resistant seal; Diameter of
container mouth must be large enough to accomodate the 4 by 8.1 Practices employed herein preserve the integrity of the
6.5 cm plastic cards (Section 7.10); each pre-labeled as material in the event that it becomes evidence. Efforts should
“POWDER SAMPLE” with unique sample identifier numbers. be made to minimize or reduce air currents that may re-
aerosolize or disturb suspected biological agents, including
7.6 Bleach Solution—Fresh pH-adjusted bleach solution
ceasing the operation of heating, ventilation, and air condition-
(household bleach diluted 1:9; pH-adjusted to 6.8-8.0) to be
ing(HVAC)andexhaustfansandotherformsofairmovement.
prepared outside of the hot zone just prior to use by (step 1)
The location of the work area should be considered prior to
mixing one part household bleach (5.25 to 6.0 % sodium
entry into the hot zone
...


This document is not an ASTM standard and is intended only to provide the user of an ASTM standard an indication of what changes have been made to the previous version. Because
it may not be technically possible to adequately depict all changes accurately, ASTM recommends that users consult prior editions as appropriate. In all cases only the current version
of the standard as published by ASTM is to be considered the official document.
Designation: E2458 − 10 E2458 − 17
Standard Practices for
Bulk Sample Collection and Swab Sample Collection of
Visible Powders Suspected of Being BiothreatBiological
Agents and Toxins from Nonporous Surfaces
This standard is issued under the fixed designation E2458; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (´) indicates an editorial change since the last revision or reapproval.
1. Scope
1.1 These practices address collection of visible powders that are suspected biothreatbiological agents and toxins from solid
nonporous surfaces using a bulk collection method, using a dry swab and laminated card, followed by a swab sampling method
using a sterile moistened swab. Bulk powder samples are collected and packaged in a manner that permits the maximum amount
of the sample to be safely transported to a reference laboratory within the Centers for Disease Control and Prevention (CDC)
national Laboratory Response Network (LRN) for confirmatory identification and safe storage. If the source of the powder is a
letter or small package, that item is also packaged in a manner that permits it to be safely transported to an LRN reference
laboratory. A sterile moistened swab may be used to collect residual powder from the nonporous surface and may be used to
conduct on-site biological assessments for the purpose of testing for biothreat agents.biological agents and toxins.
1.2 These practices are performed in coordination with the Federal Bureau of Investigation (FBI) as part of a risk assessment
including hazard assessment and threat credibility evaluation as recommended and clarified in Guide E2770. The decision to
implement these practices and collect a public safety sample will be made by members of the response community of the
jurisdiction assuming responsibility through coordination with the FBI and the receiving LRN reference laboratory.
1.3 Sample Collection Method A covers the bulk collection and packaging of suspicious visible powders that are suspected
biothreatbiological agents and toxins from solid nonporous surfaces. All samples suspected to be biothreatbiological agents and
toxins on nonporous surfaces should be collected according to Sample Collection Method A and sent to aan LRN reference
laboratory for confirmatory testing.
1.4 Sample Collection Method B covers swab sampling of residual suspicious powders that are suspected biothreatbiological
agents and toxins from solid nonporous surfaces. Swab samples can be used for on-site biological assessment; however results
from on-site biological assessments are not definitive; confirmatory testing by the LRN reference laboratory is necessary to make
public health decisions.
1.5 These practices incorporate reference guidance for packaging and transport of suspicious visible powders to comply with
all appropriate federal regulations regarding biosafety and biosecurity.
1.6 These practices should only be used to collect visible samples that are suspected biothreatbiological agents and toxins and
have been field screened according to reference guidance for explosive hazard, radiological hazard, and other acute chemical
hazards.
1.7 The values stated in SI units are to be regarded as standard. The values given in parentheses are for information only.
1.8 This standard does not purport to address all of the safety concerns associated with its use. It is the responsibility of the
user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations
prior to use.
1.9 This international standard was developed in accordance with internationally recognized principles on standardization
established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued
by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
These practices are under the jurisdiction of ASTM Committee E54 on Homeland Security Applications and are the direct responsibility of Subcommittee E54.01 on
CBRNE Sensors and Detectors.
Current edition approved Oct. 1, 2010May 15, 2017. Published November 2010June 2017. Originally approved in 2006. Last previous edition approved in 20062010 as
E2458 – 06.E2458 – 10. DOI: 10.1520/E2458-10.10.1520/E2458-17.
The CDC Laboratory Response Network is the network responsible for handling clinical specimens and environmental samples containing suspected biothreat agents.
Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States
E2458 − 17
2. Referenced Documents
2.1 ASTM Standards:
E2770 Guide for Operational Guidelines for Initial Response to Suspected Biological Agents and Toxins
F2412 Test Methods for Foot Protection
F2413 Specification for Performance Requirements for Protective (Safety) Toe Cap Footwear
2.2 Federal Government Regulations:
18 USC 175178 Prohibitions with respect to biological weapons
DOT 49 CFR, Parts 171-180 Hazardous Materials Regulations
DOT - 49 CFR 172 Subpart H, Transportation Training
DOT - 49 CFR 173 General Requirements for Shipments and Packagings
DOT - 49 CFR 178 Specifications for Packagings
EPA - 40 CFR 300 National Oil and Hazardous Substances Pollution Contingency Plan (NCP)
EPA - 40 CFR 311 Worker Protection
NRC - 10 CFR 20 Standards for Protection against Radiation
NIOSH - 42 CFR 84 Respiratory Protective Devices
OSHA - 29 CFR 1910 Subpart Z and 29 CFR 1926 Subpart Z Toxic and Hazardous Substances
OSHA - 29 1910.1096 and 29 CFR 1926.53 Ionizing Radiation
OSHA - 29 CFR 1910.120 Hazardous Waste Operations and Emergency Response (HAZWOPER) standard
OSHA - 29 CFR 1910 Subpart I (Sections 132 to 139) Personal Protective Equipment
OSHA - 29 CFR 1910.1200 Hazard Communication
2.3 Federal Guidance:
OSHA - CPL 02-02-073 Inspection Procedures for 29 CFR 1910.120 and 1926.65, Paragraph (q): Emergency Response to
Hazardous Substance Releases
NIOSH Publication No. 2009-132 Recommendations for the Selection and Use of Respirators and Protective Clothing for
Protection Against Biological Agents
FBI Laboratory Publication Handbook of Forensic Services 20032013
FBI-DHS-HHS/CDC Coordinated Document Guidance on Initial Response to a Suspicious Letter/Container with a Potential
Biological threat, November 2, 2004
CDC/NIOSH Surface Sampling Procedures for Bacillus anthracis Spores from Smooth, Non-porous Surfaces, April 26, 2012
DHS Framework for a Biothreat Field Response Mission Capability, April 2011
Sandia National Laboratories SAND2005-3237 (LBNL-54973 (II)) Guidelines to Improve Airport Preparedness Against
Chemical and Biological Terrorism
2.4 NFPA Standards:
NFPA 472 Standard for Competence of Responders to Hazardous Materials/Weapons of Mass Destruction Incidents, 20082013
Edition
NFPA 1994 Standard on Protective Ensembles for Chemical/Biological Terrorism Incidents
2.5 IATA Standards:
IATA PI 602 Infectious Diseases (Infectious Substances)
IATA PI 650 Shipping of Diagnostic Samples
IATA DGR 46th Edition, 2005
IATA DGR Addendum I, January 2005
IATA DGR Addendum II, March 2005
IATA DGR Addendum III, July 2005
2.6 ANSI Standards:
ANSI Z41-1999 American National Standard for Personal Protection - Protective Footwear
ANSI Z87.1-2003 American National Standard for Occupational and Educational Personal Eye and Face Protection Devices
ANSI Z88.2-1992 American National Standard Practices for Respiratory Protection
ANSI Z88.10-2001 American National Standard for Personal Protection - Respirator Fit Testing Methods
For referenced ASTM standards, visit the ASTM website, www.astm.org, or contact ASTM Customer Service at service@astm.org. For Annual Book of ASTM Standards
volume information, refer to the standard’s Document Summary page on the ASTM website.
Available from U.S. Government Printing Office Superintendent of Documents, 732 N. Capitol St., NW, Mail Stop: SDE, Washington, DC 20401, and also available
online from Occupational Safety and Health Administration (www.osha.gov).
Available from http://www.cdc.gov/niosh/topics/emres/surface-sampling-bacillus-anthracis.html.
Available from http://www.hsdl.org/?view&did=767721.
Available from http://share-ng.sandia.gov/news/resources/releases/2005/images/unlsand-2005-3237.pdf.
Available from National Fire Protection Association (NFPA), 1 Batterymarch Park, Quincy, MA 02269-9101.
Available from the International Air Transport Association, 800 Place Victoria, PO Box 113, Montreal-H4Z 1M1, Quebec, Canada.
Available from American National Standards Institute (ANSI), 25 W. 43rd St., 4th Floor, New York, NY 10036, http://www.ansi.org.
E2458 − 17
ANSI/ISEA Z89.1-2003 American National Standard for Personal Protection - Protective Headwear for Industrial Workers
Requirements
ANSI/Compressed Gas Association, CGA G-7.1-1997 Commodity Specification for Air
2.7 IAFC Guidance:
Model Procedures for Responding to a Package with Suspicion of a Biological Threat, October 2008
3. Terminology
3.1 Definitions:
3.1.1 aseptic technique, n—operation or performance of a procedure or method under carefully controlled conditions to reduce
the risk of exposure and prevent the introduction of unwanted material/matter (contamination) into a sample.
3.1.2 biothreatbiological agent, n—any microorganism, virus, infectious substance, or biological product that may be
engineered as a result of biotechnology, or any naturally occurring or bioengineeredmicroorganism (including but not limited to,
bacteria, viruses, fungi, rickettsiae, or protozoa), or infectious substance, or any naturally occuring, bioengineered or synthesized
component of any such microorganism, virus,microorganism or infectious substance, or biological product, capable of causing: (1)
death, disease or other biological malfunction in a human, an animal, a plant, or another living organism; (2) deterioration of food,
water, equipment, supplies, or material of any kind; or (3) deleterious alteration of the environment. 18 USC 175178
3.1.3 bulk powder, n—a visible powder, at least approximately 1 teaspoon or 5 ml 5 mL (1 teaspoon) in volume amassed or
dispersed over a limited area (optimally, area should be less than 20 by 20 cm (approximately 8 by 8 in.).
3.1.4 chain of custody, n—set of procedures and documents to account for the integrity of sample by tracking its handling and
storage from point of sample collection to final disposition of the sample.
3.1.5 cold zone, n—the uncontaminated area where workers are unlikely to be exposed to hazardous substances or dangerous
conditions; also known as Clean Zone or Support Zone. CPL 02-02-071 Directive
3.1.6 confirmatory analysis, n—a test or a series of assays that definitively identifies the presence of a suspected substance or
agent.
Available from International Association of Fire Chiefs (IAFC), 4025 Fair Ridge Drive, Suite 300 Fairfax, VA 22033, http://www.iafc.org.
3.1.6.1 Discussion—
Confirmatory analysis of a biothreat biological agent for public health action can be performed only by an LRN national or
reference laboratory.
3.1.7 decontamination, n—the physical or chemical process, or both, of reducing and preventing the spread of contaminants
from people, animals, the environment, or equipment involved at hazardous materials/weapons of mass destruction (WMD)
incidents. NFPA
3.1.8 field screening, n—field measurements utilized early in the site assessment process response to define and delineatechar-
acterize the contaminants present, potential hazards present, including corrosive, flammable, volatile, radioactive, or oxidizer
hazards, and to support tactical decision making andto address operational safety measures.
3.1.8.1 Discussion—
Field screening does not include measurements of biological properties, which is termed on-site biological assessments (see
3.1.12).
3.1.9 hazard, n—something that is potentially dangerous or harmful, often the root cause of an unwanted outcome; a danger or
peril. NIMS
3.1.10 hot zone, n—the area, located on the site where contamination is either known or expected and where potential for
greatest exposure exists; also known as Exclusion Zone or ExZ. CPL 02-02-071 Directive
3.1.11 incident commander (IC), n—the individual responsible for all incident activities, including the development of strategies
and tactics and the ordering and release of resources.
3.1.11.1 Discussion—
The IC has overall authority and responsibility for conducting incident operations and is responsible for the management of all
incident operations at the incident site. NIMS
E2458 − 17
3.1.12 on-site biological assessment, n—measurements of properties inherent to biological materials performed in the field
using rapid, field-based procedures and assays.
3.1.13 personal protective equipment (PPE), n—equipment provided to shield or isolate a person from the chemical, biological,
physical, and thermal hazards that can be encountered at hazardous materials/weapons of mass destruction (WMD) incidents.
NFPA
3.1.14 presumptive test, n—non-definitive test used to evaluate a material for the presence of a substance or agent, or the
presence of signatures of a substance or agent.
3.1.15 risk, n—the probability of suffering a loss or harm or injury; peril.
3.1.16 toxin, n—the toxic material or product of plants, animals, microorganisms (including but not limited to, bacteria, viruses,
fungi, rickettsiae, or protozoa), or infectious substances, or a recombinant or synthesized molecule, whatever their origin and
method of production, and includes: (1) any poisonous substance or biological product that may be engineered as a result of
biotechnology produced by a living organism; or (2) any poisonous isomer or biological product, homolog, or derivative of such
a substance (18 USC 178).
3.1.17 threat, n—an indication of possible violence, harm, or danger and may include an indication of intent and capability.
NIMS
3.1.18 warm zone, n—the transition area between the Exclusion Zone (ExZ or hot zone) and the Support Zone (SZ or cold zone)
used to reduce and limit the amount of contamination on people and equipment, and in the air, water, and soil that may be
transferred into nonhazardous areas; the CRZ contains decontamination facilities, and functions as a buffer zone surrounding the
ExZ; also known as the contamination reduction zone or CRZ. CPL 02-02-071 Directive
3.1.19 weapon of mass destruction (WMD), n—any weapon or device that is intended, or has the capability, to cause death or
serious bodily injury to a significant number of people through the release, dissemination, or impact of (1) toxic or poisonous
chemicals or their precursors; (2) a disease organism; or (3) radiation or radioactivity. U.S. Code Title 50, Ch. 40, Sect. 2302, War
and National Defense Definitions
3.2 Acronyms:
3.2.1 AHJ—Authority Having Jurisdiction
3.2.2 ANSI—American National Standards Institute
3.2.3 ASTM—American Society for Testing and Materials
3.2.4 CDC—Centers for Disease Control and Prevention
3.2.5 CFR—Code of Federal Regulations
3.2.6 CRZ—Contamination Reduction Zone
3.2.7 CST—Civil Support Team
3.2.8 DHS—Department of Homeland Security
3.2.9 DOT—Department of Transportation
3.2.10 EOC—Emergency Operations Center
3.2.11 EPA—Environmental Protection Agency
3.2.12 ExZ—Exclusion Zone
3.2.13 FBI—Federal Bureau of Investigation
3.2.14 FEMA—Federal Emergency Management Agency
3.2.15 HAZMAT—Hazardous Materials
3.2.16 HHS—Health and Human Services
3.2.17 IAFC—International Association of Fire Chiefs
3.2.18 IATA—International Air Transport Association
3.2.19 IC—Incident Commander
3.2.20 ICS—Incident Command System
3.2.21 IEC—International Electrotechnical Commission
3.2.22 ISEA—International Safety Equipment Association
3.2.23 ISO—International Organization for Standardization
3.2.24 LRN—Laboratory Response Network
3.2.25 MACS—Multiagency Coordination System
3.2.26 NFPA—National Fire Protection Association
E2458 − 17
3.2.27 NIMS—National Incident Management System
3.2.28 NIOSH—National Institute for Occupational Safety and Health
3.2.29 NRC—Nuclear Regulatory Commission
3.2.30 OSHA—Occupational Safety and Health Administration
3.2.31 PBS—Phosphate Buffered Saline
3.2.32 PPE—Personal Protective Equipment
3.2.33 SZ—Support Zone
3.2.34 USAR—US&R—Urban Search and Rescue
3.2.35 WMD—Weapons of Mass Destruction
4. Significance and Use
4.1 These practices should be used only to collect visible samples that are suspected biothreatbiological agents and toxins and
have been field screened as defined by the FBI-DHS-HHS/CDC Coordinated Document for explosive hazard, radiological hazard,
and other acute chemical hazards.
4.2 These practices provide standardized methods for collecting, packaging, and transporting suspicious visible powder samples
that are suspected biothreat agents. biological agents and toxins. Collection of a bulk powder material from a nonporous surface
using a sterile swab and laminated card as the collection devices to move the material into a container will depend on several
factors, including (but not limited to): (1) amount of visible powder present; (2) sample composition; (3) choice of collection
device; (4) size and shape of the collection container; (5) ability of the powder to become aerosolized; (6) texture and porosity of
the surface; (7) humidity; (8) air movement; and (9) electrostatic properties of powders and collection tools/containers.
4.3 Similarly, these practices standardize methods for sampling suspicious visible powders for on-site analysis, although wipe
and swab sampling is often employed in the field for subsequent LRN reference laboratory analysis. The ability to collect suitable
samples from nonporous surfaces using a sterile moistened swab will depend on the following factors: (1) swabbing procedure;
(2) swab material; (3) sample composition; and (4) texture of the surface.
4.4 These practices standardize suspicious powder collection and packaging procedures and swab sampling procedures in order
to reduce exposure risk, to reduce variability associated with sample handling and sample analysis, and to increase reliability of
sampling visible powder samples from nonporous surfaces.
4.5 The bulk sample collection practice and the swab sampling practice are recommended for collecting amassed or dispersed
powder samples from all nonporous surfaces on which the suspicious powder sample is clearly visible.
4.6 These practices are not recommended for samples on porous materials such as upholstery, carpeting, air filters, or ceiling
tiles.
4.7 These practices are recommended for collecting visible powders where the bulk of the powder sample is amassed or
dispersed over a limited area (optimally, area should be less than 20 by 20 cm (approximately 8 by 8 in.) or 400 cm (approximately
64 in. ).
4.8 These practices are to be performed by personnel who are adequately trained to work with hazardous materials in the hot
zone (see NFPA 472, or OSHA - 29 CFR 1910.120). Personnel performing collection or screening under these practices shall be
adequately trained in the use of sampling equipment, materials, and procedures. This includes personnel performing the prior initial
chemical and radiological screening. Personnel should use the appropriate level of personal protective equipment (PPE) to mitigate
hazards during collection and screening. Personnel performing collection or screening under these practices shall be aware of
evidence preservation and sampling procedures (NFPA 472 section 6.5).
4.9 These standard practices should be used in accordance with Guide E2770 for best practices for planning, training and
evaluation of competency.
SAMPLE COLLECTION METHOD A—BULK SAMPLE COLLECTION FOR LABORATORY ANALYSIS
5. Scope of Method A
5.1 This sample collection method applies to the bulk collection and packaging of suspicious visible powders that are suspected
biothreat agents biological agents or toxins, or both, from solid nonporous surfaces.
5.2 These practices are performed in coordination with the FBI and receiving LRN reference laboratory after a risk assessment
including a hazard assessment and threat credibility evaluation is conducted and the sample is deemed potentially to be a credible
threat as recommended and clarified in Guide E2770.
E2458 − 17
5.3 This sample collection method applies to suspicious visible powders that are amassed or dispersed in a limited area where
the bulk of the powder sample is in an area that is less than 20 by 20 cm (approximately 8 by 8 in.) or 400 cm (approximately
64 in. ).
5.4 These practices should be used only to collect samples that are suspected biothreat hazards and biological agent and toxin
hazards that have been field screened as defined by the FBI-DHS-HHS/CDC Coordinated Document for explosive, radiological,
and chemical hazards.
6. Summary of Sample Collection Method A
6.1 A visible powder sample that is a suspected biothreat agent biological agent or toxin, or both, and its source should be field
screened for non-biological hazards as defined in the FBI-DHS-HHS/CDC Coordinated Document and according to the reference
guidance including appropriate NFPA documents. Non-biological hazards include explosive, radiological, and chemical hazards.
The visible powder sample, amassed or dispersed in a limited area, is collected from a nonporous surface using a swab and a
laminated card to move the sample into a sterile dry collection container that is held close to the surface.
6.2 The method provides guidance on performing these procedures in a manner that will minimize sample loss and
aerosolization of the powder. The bulk powder sample and swab are sent to aan LRN reference laboratory for confirmatory
analysis.
7. Sampling and Packaging Equipment and Supplies
7.1 Personal Protective Equipment—Level A, B, or C personal protective equipment ensembles as indicated (see Section 2 for
additional guidance, including OSHA - 29 CFR 1910.120 Appendix B and NFPA 1994).
7.2 Clean drop cloth to create a cleanan isolated work area.
7.3 Sample Transport Container—Bucket or large heavy duty plastic bag.bag used to transport the samples and materials from
the hot zone through to the decontamination line.
7.4 Non-powdered Nitrile or Vinyl Examination Gloves.
7.5 Two Sterile Polypropylene Wide-mouth Screw-capped Sample Collection Containers (Sample Containers)—Containers must
possess a leak-resistant seal; Diameter of container mouth must be large enough to accomodate the 4 by 6.5 cm plastic cards
(Section 7.10); each pre-labeled as “POWDER SAMPLE” with unique sample identifier numbers.
7.6 Bleach Solution—Fresh pH-adjusted bleach solution (household bleach diluted 1:9; pH-adjusted to 6.8-8.0) to be prepared
outside of the hot zone just prior to use by (step 1) mixing one part household bleach (5.25 to 6.0 % sodium hypochlorite) with
5 parts water (v/v);(volume/volume); (step 2) adding 1 part white vinegar; (step 3) adding 3 parts of additional water.
7.7 Labeling or Marking Tape.
7.8 Solvent-resistant Indelible Marker.
7.9 Sterile Culture Swabs, (rayon, macrofoam, or polyester) individually packaged and sterile, self-contained in sealed plastic
tubes, with absorbent material wrapped around one end of a plastic stick, unopened.
7.10 Two at least 4 by 6.5 cm (approximately 1.5 by 2.5 in. ) Sterile Plastic Laminated Cards.
7.11 Six 1-gal Sealable Plastic Bag(s)—Both bags with sliding lock and Trademark Whirl-Pak bags are not recommended for
this purpose since they may not seal completely; the use of colored or opaque bags is discouraged because it makes viewing of
the sample more difficult once transported back to the laboratory in the CDC Laboratory Response Network.
7.12 Bucket, or other container marked “BIOHAZARD WASTE”.
7.13 1-gal Sealable Plastic Bag(s), pre-labeled as “BIOHAZARD WASTE”.
7.14 Field Screening Results Form—See example in Appendix X1.
7.15 Sample Collection Sheet—See example in Appendix X1. Note that a single sample collection sheet can be used for all items
collected at a single location including primary source, swab, and powder sample(s).
7.16 Chain-of-Custody Form—See example in Appendix X1.
7.17 Two Plastic Transparent Document Pouches, with adhesive on back.
7.18 Durable Hard-sided Outer Container, with lid or screw cap, for sample transport (such as metal can with lid, or plastic
container with lid).
Additional information about decontamination with pH-adjusted bleach solution is available at www.epa.gov/opp00001/factsheets/chemicals/bleachfactsheet.htm
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