FDA Device recall Z-2623-2026
GC Agar Base (150mm) 10/PK R04030
- FDA Device
- Class II
- ongoing
- Published 2026-07-08
On 2026-07-08 the FDA classified a Class II recall of GC Agar Base (150mm) 10/PK R04030 by Remel, citing reduced or no recovery of some strains of Neisseria gonorrhoeae.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2623-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-06-03 |
| Published | 2026-07-08 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Remel |
| Distribution | US |
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.
Identifiers
| code_info | R01460 - GC Agar Base (100mm) 10/PK UDI-DI 848838001796 Lots 338950 356898 359912 365679 371863 376799 382136 384712 39…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 history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2623-2026%22
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