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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

Becton Dickinson & Co.: Product service credentials used by some BD technical support teams to access certain BD products were accessed by an unauthorized actor. Until these product service credentials are updated, there is a risk of unauthorized access that may impact the confidentiality, integrity and/or availability of the relevant products and associated data.

Agency Publication Date: October 23, 2025
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Summary

Becton Dickinson & Co. (BD) has issued a recall for approximately 2,050 units of its EpiCenter Microbiology Data Management System, including various computer models like the OptiPlex and NUC systems. This recall follows an incident where an unauthorized actor accessed product service credentials used by BD technical support teams. BD is working to update these credentials to prevent further risk of unauthorized access to the systems and sensitive microbiology data.

Risk

An unauthorized actor could exploit these stolen credentials to remotely access the microbiology data management system. This poses a significant risk to the confidentiality, integrity, and availability of patient diagnostic data and laboratory results.

What You Should Do

  1. Identify if your system is affected by checking the Catalog Number (441002, 441421, 445398, or 443971) and matching your device's Serial Number against the extensive list provided in the recall notice.
  2. Ensure your EpiCenter system is behind a secure firewall and not directly accessible via the public internet.
  3. Monitor for any unauthorized changes to the system or data and follow any specific patching or credential update instructions provided directly by BD technical support.
  4. Contact BD Technical Support or your local BD representative to confirm when your specific product service credentials have been successfully rotated or updated.
  5. For additional questions or to report suspected unauthorized access, contact the FDA device recall line or BD customer service.

Your Remedy Options

๐Ÿ“‹Other Action

Credential update and security patch

How to: Until product service credentials are updated, there is a risk of unauthorized access. BD is working to update these credentials.

Affected Products

Product: BD EpiCenter Microbiology Data Management System - Computer System Epicenter F/G
Model / REF:
441002
UPC Codes:
00382904410025
Lot Numbers:
MXL8503690
5xlz833
HCT26Q3
FB3D7F3
MY816005EF
EPSN0443
EPSN0445
EPSN0496
EPSN0500
4WMW9R2
EPSN0509
EPSN0480
MXL8501ST4
Product: BD EpiCenter Microbiology Data Management System - COMPUTER OPTIPLEX EPICENTER SPARE
Model / REF:
441421
UPC Codes:
00382904414214
Lot Numbers:
941TSR1
5GFG64J
FWCF15J
60SQY4J
2GFG64J
Product: BD EpiCenter Microbiology Data Management System - Generic NUC 2
Model / REF:
445398
UPC Codes:
00382904453985
Lot Numbers:
G6MY934003YV
G6MY84600PDX
G6MY9340042E
G6MY72900GD
G6MY93400454
G6MY9340044S
G6MY9340045Z
Product: BD EpiCenter Microbiology Data Management System - Nuc 5i5 Os Image Bow 2.X
Model / REF:
443971
UPC Codes:
00382904439712
Lot Numbers:
G6MY934003LM
G6MY934004BS
G6MY803008JK
G6MY934003J4
G6MY83700CQY
G6MY84200M2R
G6MY934003U2
G6MY737008M7

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97479
Status: Active
Manufacturer: Becton Dickinson & Co.
Manufactured In: United States
Units Affected: 6 products (2,050 units; 177 units; 1,086 units; 62 units; 4,283 units; 38 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.