ClearanceBrief
Recall Z-0592-2025 ยท LON System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

Becton Dickinson & Co.

BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624

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
Quantity4,411 units (567 US, 3,844 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

K020321BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM
Becton, Dickinson & CO, May 23, 2002
K040099BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM
Becton, Dickinson & CO, Mar 19, 2004
K131331BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM - VANCOMYCIN (0.5-32 UG/ML)
Becton, Dickinson & CO, Jul 10, 2013