Official recall record
BD BACTEC™ MGIT™ 960 PZA Kit
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-11-14
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
This a follow-up letter to previous field safety notifications IDS-24-5091/IDS-25-5091-EXP. BD is notifying customers that it has resumed production of a modified version of the BD BACTEC™ MGIT™ 960 PZA Kit which includes modified inoculation methods and reduced shelf-life.
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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