Class IIOngoingZ-2623-2026
Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030
Reduced or no recovery of some strains of Neisseria gonorrhoeae.
- For Isolation Of Pathogenic Neisseria Culture Media
- Under Investigation by firm
Remel, IncKSJul 8, 2026
Remel, Inc recalls
The FDA has posted 12 enforcement recalls from Remel, Inc since 2025, none of them Class I (most serious). Most recent report: Jul 8, 2026.
Class II: 12
Latest recalls
View all 12 in the recall browser →Class IIOngoingZ-1806-2026
Remel, Inc recalls Yeastone Broth
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.
- Antifungal Susceptibility Test Plate
- Under Investigation by firm
Remel, IncKSApr 22, 2026
Class IIOngoingZ-1474-2026
Remel, Inc recalls Campy CVA Medium 100/PK
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- Selective And Non-Differential Culture Media
- Under Investigation by firm
Remel, IncKSMar 4, 2026
Class IIOngoingZ-0585-2026
Remel, Inc recalls 1. CAMHB W/LHB
Products may contain contamination, which may result in a darker or brown media color.
- Mueller Hinton Agar/Broth Antimicrobial Susceptibility Test Culture Media
- Under Investigation by firm
Remel, IncKSDec 3, 2025
Class IIOngoingZ-2223-2025
Remel, Inc recalls Blood Agar
The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Non-Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSAug 6, 2025
Class IIOngoingZ-2226-2025
Remel, Inc recalls Blood/MacConkey Biplate 100/PK
The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSAug 6, 2025
Class IIOngoingZ-2224-2025
Remel, Inc recalls Strep Selective II Agar
The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSAug 6, 2025
Class IIOngoingZ-2225-2025
Remel, Inc recalls Blood/EMB
The products may contain surface and subsurface contamination of Listeria monocytogenes.
- Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSAug 6, 2025
Class IIOngoingZ-1947-2025
Remel, Inc recalls Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Ly…
Product may have an off color affecting perfomance
- Manual Antimicrobial Susceptibility Test Systems
- Under Investigation by firm
Remel, IncKSJun 18, 2025
Class IIOngoingZ-1395-2025
Remel, Inc recalls Zebra Thermal Barcode Printer GX430t
Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.
- Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
- Nonconforming Material/Component
Remel, IncKSMar 26, 2025
Class IIOngoingZ-1201-2025
Remel, Inc recalls remel BLOOD AGAR EMB AGAR BIPLATE
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
- Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSFeb 26, 2025
Class IIOngoingZ-1200-2025
Remel, Inc recalls remel BLOOD AGAR MacCONKEY AGAR BIPLATE
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
- Selective And Differential Culture Media
- Under Investigation by firm
Remel, IncKSFeb 26, 2025
Firm name as filed with the FDA: “Remel, Inc”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.