Becton Dickinson recalls BD MAX System for in vitro diagnostics due to potential unauthorized access to product service credentials, risking data confidentiality and security.
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.
Becton Dickinson is recalling its BD MAX System for in vitro diagnostic use because unauthorized access to product service credentials could compromise data confidentiality and security. This recall affects specific model numbers and serial numbers listed in the notice.
Unauthorized access to product service credentials could allow attackers to impact the confidentiality, integrity, or availability of the BD products and associated data. This risk arises from outdated credentials used by some technical support teams.
Users of the BD MAX System for in vitro diagnostics are affected, particularly those with the specific catalog numbers and serial numbers listed in the recall notice.
Check for catalog numbers 44191609 and 441927, and serial numbers starting with UDI/DI codes like 00382904419165 or 00382904419271 as listed in the recall notice.
Identify your BD MAX System's catalog number and serial numbers to confirm if it is affected by this recall.
Becton Dickinson is recalling the BD MAX System due to potential unauthorized access to product service credentials, which could compromise data confidentiality and security.
The recall affects BD MAX System with catalog numbers 44191609 and 441927, and specific serial numbers listed in the notice.
Yes, check your product's catalog number and serial numbers to see if it is affected; no specific action is required beyond verification.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-0238-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-0238-2026 from Becton Dickinson. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
