FDAJuly 12, 2017device

VITEK¿ 2 Compact 15, REF numbers: 27415 and 27415R software and reagent cards designed for the identification (ID) and antimicrobial susceptibility testing (AST) of bacteria and yeast.

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

The hazard

Customers have reported that some VITEK¿ 2 cards are staying in preliminary status, not finalizing after ejection from the instrument, and not allowing cards in subsequent carousel slots to be processed. The issue was reported to occur on VITEK¿ 2 Compact 15 and Compact 30 systems following a system software update to version 8.01.

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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