FDAApril 13, 2017device

ETEST OXACILLIN OX 256 US F100 In vitro diagnostic, a quantitative technique for determining the antimicrobial susceptibility of bacteria species.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux sabiomerieux

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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