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Remel, Inc

Remel, Inc: 3 recalls listed since February 2026 across FDA.

By year

  • 20263

By agency

  • FDA3

By category

  • Medical Device3

All recalls (3)

Remel GC Agar Base

GC Agar Base may have reduced or no recovery of some strains of Neisseria gonorrhoeae.

Moderate risk, FDA, , Device defect

Remel Yeastone Broth

Yeastone Broth may report incorrect AST results during quality control, potentially causing delayed response or need to change antifungal agent.

Moderate risk, FDA, , Device defect

Remel Campy CVA Medium

Campy CVA Medium may have low recovery of Campylobacter Jejuni.

Moderate risk, FDA, , Device defect
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