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Medical Device

VITEK 2 AST-N447 TEST KIT Product reference 424620

Recall date: 2026-07-15 · Source: FDA_DEVICE
Brand / Firm
Biomerieux Inc
Product
VITEK 2 AST-N447 TEST KIT Product reference 424620
Reason for recall
Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.
Units affected
45,900 cards
Description
VITEK 2 AST-N447 TEST KIT Product reference 424620
View official recall notice →