Official recall record
BD BACTEC MGIT 960 PZA Kit And Susceptibility Test Medium
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-07-31
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Through internal BD complaint trending and subsequent internal raw material testing it was identified that the BD BACTEC™ MGIT™ 960 PZA Kits, listed in attachment 1 may intermittently produce falsely resistant results for pyrazinamide (PZA) during susceptibility testing of mycobacterium tuberculosis isolates. Recall start date: July 18, 2024
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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