Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2023-2025 — BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tuberculosis, from culture to pyrazinamide (PZA).

U.S. FDA — Device Enforcement · United States · 2025-05-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2023-2025
Date of alert
2025-05-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Co.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0038290245128
Reported risk: BD has received additional complaints of intermittent false resistance results for PZA during susceptibility testing of Mycobacterium tuberculosis isolates.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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