Remel, Inc recalls GC Agar Base
- Recalling company
- Remel, Inc
- 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.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jun 3, 2026
- Reported
- Jul 8, 2026
- Distribution
- Worldwide distribution - US Nationwide and the countries of Canada, Singapore, and the United Kingdom.
- Status
- Ongoing
- Quantity
- 1573
- Lot / codes
- R01460 - GC Agar Base (100mm) 10/PK UDI-DI 848838001796 Lots 338950 356898 359912 365679 371863 376799 382136 384712 393488 396333 402458; R04030 - GC Agar Base (150mm) 10/PK UDI-DI 848838004469 Lots 336864 345992 348754 359925 367829 374235 376786 381488 385224 391312 393478
- Company location
- Lenexa, KS
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2623-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2623-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.