Becton Dickinson & Co.: System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

Recalling firm
Becton Dickinson & Co.
Product
BD Phoenix Panel NMIC-306. Catalog Number: 449292.
Reason
Potential for quality control failures with Klebsiella pneumoniae ATCC BAA-1705 when using the CPO Ambler classification feature.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-08-13
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
US Nationwide distribution.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2c6aa90d-fd51-4934-aebb-c2a68fbd04d4