HIGH
FDA DEVICE
GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
Remel
Reduced or
Brand hub
Remel Recalls
3 recalls found for Remel. Check current safety alerts and related brands before using affected products.
- Active recalls
- 3
- Pages
- 1
HIGH
FDA DEVICE
Yeastone Broth, 11ML, 10/BOX YY3462
Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.
Remel
Products may
Health & Personal Care
HIGH
FDA DEVICE
Remel Recalls Campy CVA Medium Over Low Recovery Rates
Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.
Remel
Customer complaints
Brand Statistics
Total Recalls
3
Pages
1