FDAMay 20, 2025device

BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.

What to do

FDA enforcement status: Ongoing

Brands named

becton dickinsonbectonbecton dickinson

UPCs

0038290245128

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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