Becton Dickinson & Co.: System, Test, Automated, Antimicrobial Susceptibility, Short Incubation
Recall Summary BD Phoenix Panel NMIC-312 (Catalog Number 449082), a laboratory test system used to identify antibiotic resistance in bacteria, is being recalled nationwide because it may fail quality control checks when testing a specific strain of Klebsiella pneumoniae bacteria using the CPO Ambler classification feature. This could result in inaccurate test results. The recall affects laboratories and healthcare facilities across all U.S. states and Washington, D.C.
- Recalling firm
- Becton Dickinson & Co.
- Product
- BD Phoenix Panel NMIC-312. Catalog Number: 449082.
- 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/e7d3f0fa-612e-49c4-924a-b9afefeaedfe