Official recall record
BBL Sensi-Disc Antimicrobial Susceptibility Test Discs
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-01-10
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
BD confirmed through a recent evaluation of BD BBL™ Sensi-Disc™ product that twenty-eight (28) out of thirty (30) antimicrobial discs showed reproducibility, accuracy, and/or quality control (qc) failures when tested with Haemophilus spp. Testing with other bacterial pathogens (where indicated) is not affected. Recall Start Date: December 29, 2023
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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