Class II

Medical Device Recall: GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460

Remel, Inc · June 3, 2026

Reason for Recall

Reduced or no recovery of some strains of Neisseria gonorrhoeae.

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, Singapore, and the United Kingdom.

States Affected

NATIONWIDE

Quantity Affected

1573

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2623-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Remel, Inc Medical Device Recall: GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460 | SafeCheck