Official recall record
Vitek 2 Software Version 9.01/9.02
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-07-12
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Biomerieux has become aware that when using the Firefox web browser to access the Vitek® 2 software versions 9.01-9.02 and editing the accession ID on an isolate, or a batch of isolates, an anomaly can occur. The Vitek® 2 software version are KIT, UPDT VTK2 09.01/ 09.02 (clinical - ref. 423487) and KIT, UPDT VTK2 9.01/9.02 (industry - ref.423585). Recall start date: June 28, 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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