Becton Dickinson & Co.: Medical Device Recalls in 2023

According to to data from the FDA, there were 4 medical device recalls made by Becton Dickinson & Co. in 2023. See the details of the recalls below.

You can see similar recalls for other firms.

• BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous qualitative detection and differentiation of SARS-CoV-2 nucleocapsid antigen and influenza A and/or B Catalog Number: 256088
• BD Synapsys Informatics Solution, Catalog Number 444150
• BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro diagnostic medical device intended to automate specimen processing according to user-defined procedures and protocols. Catalog (Ref) No. : 447213
• BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023