# FDA device recall: VITEK 2 AST-N447 TEST KIT  Product reference 424620

> recall · VERIFIED · 2026-06-04

Firm: Biomerieux Inc · Class II · Potential for false resistant carbapenem and/or cephalosporin results when analyzing samples with kits from affected lot that have pouch foil fractures.

- Company: Biomerieux Inc
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.