FDAOctober 11, 2017device

VITEK2 GP-ID, REF 21342 IVD

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

The hazard

Customers have reported, and an internal investigation has confirmed, occurrences of atypical negative O129R reactions for Enterococcus casseliflavus ATCC)R) 700327(TM) in association with three (3) VITEK(R) 2 GP ID Lots, causing failure of the Quality Control (QC) testing for the VITEK(R) 2 GP ID card. In accordance with the VITEK(R) 2 GP ID Instructions For Use, the expected O129R reaction for ATCC(R) 700327(TM) strain is positive. As a precaution, bioM¿rieux is also including in the scope of this notice all GP ID card lots manufactured with the same raw materials.

What to do

FDA enforcement status: Terminated

Brands named

biomerieux

UPCs

03573026131920

Recall history

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

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