bioMerieux, Inc.: Medical Device Recalls in 2022

According to to data from the FDA, there were 20 medical device recalls made by bioMerieux, Inc. in 2022. See the details of the recalls below.

You can see similar recalls for other firms.

• NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.
• VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9
• VIDAS DEX@, Dimer Exclusion II, REF 30455-01
• VIDAS Mumps IgG (MPG), REF 30218
• VIDAS SARS-COV-2 IgM, Ref 423833-01
• VIDAS Lyme IgM II (LYM), REF 416436
• VIDAS RUB IgG (RBG), REF 30226
• VIDAS TOXO IgG Avidity (TXGA), REF 30222-01
• VIDAS LH, REF 30406-01
• VIDAS Clostridium Difficile GDH, REF 30125-01
• VIDAS B.R.A.H.M.S. PROCALCITONIN PCT, REF 30450-01
• VIDAS FSH, REF 30407-01
• VIDAS Clostridium Difficile Toxin A&B, CDAB,REF 30118-01
• VIDAS Estradiol II, REF 30431-01
• VIDAS Measles IgG (MSG), REF 30219
• VIDAS PRG Progesterone, REF 30409-01
• VIDAS SARS-COV-2 IgG, Ref 423834-01
• VIDAS Lyme IgG II (LYM), REF 417401
• VITEK 2 Systems and VITEK 2 with MYLA.
• VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.