Biomerieux product recalled over mold contamination
- Recall date
- March 27, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Biomerieux Inc recalls Vitek 2 AST-YS06 REF 412 610, Fungal Susceptibility Card, 20 cards per carton, IVD. Intended for use with the Vitek 2 S…
- Recall number
- Z-1601-2015
- FDA classification
- Class II
- Brand / firm
- Biomerieux Inc
- Sold / distributed
- Distributed only to foreign subsidiaries and distributors, including Canada and Mexico.
Why it was recalled
The test kits have Out-of-Range-Low (OORL) Flucytosine QC results for Candida krusei ATCC 6258
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Vitek 2 AST-YS06 REF 412 610, Fungal Susceptibility Card, 20 cards per carton, IVD. Intended for use with the Vitek 2 Systems in clinical laboratories as an in vitro test to determine the susceptibility of clinically significant yeasts to antifungal agents when used as instructed.
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