# FDA device recall: GC Agar Base (150mm) 10/PK R04030;  GC Agar Base (100mm) 10/PK R01460

> recall · VERIFIED · 2026-06-03

Firm: Remel, Inc · Class II · Reduced or no recovery of some strains of Neisseria gonorrhoeae.

- Company: Remel, Inc
- Sector: diagnostics
- 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.