FDA recall Z-2623-2026

Remel, Inc · Class II · device

Product

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

Reason for recall

Reduced or no recovery of some strains of Neisseria gonorrhoeae.

Distribution

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

Key facts

Status
Ongoing
Initiation date
2026-06-03
Report date
2026-07-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lenexa, KS, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2623-2026