ClearanceBrief
Recall Z-0590-2025 ยท OZN C. Difficile Toxin Gene Amplification Assay

Becton Dickinson & Co.

BD MAX System, BD MAX Instrument Version or Model: 441916 Catalog Number: 441916

DateDec 3, 2024 (initiated Oct 31, 2024)
StatusOpen, Classified
ReasonBD confirmed that 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.
Root causeSoftware design
ActionOn October 31, 2024 URGENT" MEDICAL DEVICE PRODUCT CORRECTION letters were sent to consignees. IT, Safety and Security Actions to be Taken: BD encourages customers to follow best practices for maintaining strong security measures to protect hospital networks and medical devices including: "Ensure access to potentially vulnerable devices is limited to authorized personnel "Inform authorized users of issue, and ensure all relevant passwords are tightly controlled "Monitor and log network traffic attempting to reach medical device managementenvironments for suspicious activity "Where possible, is
Quantity2,537 units (876 US, 1,661 OUS)
DistributionWorldwide distribution - US Nationwide and the countries of Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Benin, Bhutan, Bolivia, Bosnia and Herzegovina, Botswana, Brazil, Brunei, Bulgaria, Burkina Faso, Burundi, Cambodia, Cameroon, Canada, Chile
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K111860BD MAX GBS ASSAY, BD MAX INSTRUMENT
Becton, Dickinson & CO, Feb 16, 2012
K120138BD MAX MRSA ASSAY, BD MAX INSTRUMENT
Bd Diagnostics (Geneohm Sciences Canada, Inc), Jul 5, 2012
K130470BD MAX CDIFF ASSAY, BD MAX INSTRUMENT
Geneohm Sciences Canada, Inc. (Bd Diagnostics), Apr 2, 2013