Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic. Recalled by BioMerieux SA Due to QC results were out of range resulting in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact BioMerieux SA directly.
Affected Products
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Quantity: 674
Why Was This Recalled?
QC results were out of range resulting in false resistant strains.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About BioMerieux SA
BioMerieux SA has 45 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report