Recall Z-2623-2026— Remel, Inc
Class II · Ongoing
Class II FDA medical device recall by Remel, Inc, initiated 2026-06-03. Product: GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460. Reason: Reduced or no recovery of some strains of Neisseria gonorrhoeae..
- Recalling firm
- Remel, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2026-06-03
- Firm location
- Lenexa, KS, United States
Product description
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Reason for recall
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
Data sourced from openFDA. This site is unofficial and independent of the FDA.