Becton Dickinson & Co.: Medical Device Recalls in 2022
Updated on March 25, 2026.
According to to data from the FDA, there were 4 medical device recalls made by Becton Dickinson & Co. in 2022. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10
- BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalog Number: 256066
- BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267
- BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative anaerobic gram-positive bacteria of human origin with selected antimicrobial agents when used with the BD Phoenix Automated Microbiology System. Catalog (Ref) Number: 448607