Remel, Inc

Devices recall · Z-2623-2026

Reason for recall

Reduced or no recovery of some strains of Neisseria gonorrhoeae.

Product description

GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460

Recalling firm

Remel, Inc

Product quantity

1573

Lot / code info

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

Distribution

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

Recall initiated

2026-06-03

Status

Ongoing

Location

Lenexa, KS, United States

Voluntary / mandated

Voluntary: Firm initiated

Initial notification

Letter

Data from official federal safety records. Updated periodically. Verify on FDA.gov