FDAJune 12, 2015device

Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.

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

The hazard

QC results were out of range resulting in false resistant strains.

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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