- Recalling firm
- Remel, Inc
- Reason for recall
- Reduced or no recovery of some strains of Neisseria gonorrhoeae.
- Affected products (lot / model / serial)
- 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
- Units affected
- 1573
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Canada, Singapore, and the United Kingdom.
- Firm location
- Lenexa, KS, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2623-2026
- Recall initiated
- June 3, 2026
- FDA classification date
- June 30, 2026
- FDA report date
- July 8, 2026
- FDA event ID
- 99132
- Last updated on HTM Vibe
- July 23, 2026