FDAJune 24, 2021device

ETEST IMIPENEM RELEBACTAM. in vitro diagnostic

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

The hazard

Major errors (Resistant result instead of Susceptible result) were observed with Pseudomonas aeruginosa strains.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

Recall history

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

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