Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ETEST OXACILLIN OX 256 WW F100 In vitro diagnostic Recalled by BioMerieux SA Due to QC failures (MIC out of range high) for...
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 OXACILLIN OX 256 WW F100 In vitro diagnostic, a quantitative technique for determining the antimicrobial susceptibility of bacteria species.
Quantity: 1585 units
Why Was This Recalled?
QC failures (MIC out of range high) for S.aureus ATCC 29213 strain on ETEST OX 256 (OXACILLIN) Foam packaging (Ref. 520558, 520518) reported. The product behavior could lead to False Resistant results.
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