FDA Class II · Medical device · July 8, 2026
GC Agar Base (150mm) 10/PK R04030 recall — Remel, Inc
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
Official ID Z-2623-2026 · Official record ↗
Remel recalls
Recall found. Remel is named in FDA Class II recall Z-2623-2026 covering GC Agar Base (150mm) 10/PK R04030. Hazard: Reduced or no recovery of some strains of Neisseria gonorrhoeae. Identifying details: 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. Status: Ongoing.
Models with recalls
All Remel recalls
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- FDA — food, drugs, medical devices ↗ (aggregated here)
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- Recalls.gov — the U.S. government’s all-agency portal ↗
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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.