Remel recalls

13 official recalls and safety alerts involving Remel since 2022-03, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Remel or the relevant agency.

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460

    Reduced or no recovery of some strains of Neisseria gonorrhoeae.

    FDA · DeviceRemel, IncWorldwide distribution - US Nationwide and the countries of Canada, Singapore,…Official notice →
  3. 2026-04-22
  4. US
    Drugs & medicalClass II

    Remel, Inc recalls 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.

    FDA · DeviceRemel, IncWorldwide distribution - US Nationwide and the countries of Canada, Vietnam,…Official notice →
  5. 2026-03-04
  6. US
    Drugs & medicalClass II

    Remel, Inc recalls Campy CVA Medium 100/PK, R01272

    Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

    FDA · DeviceRemel, IncUS Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.Official notice →
  7. 2025-12-03
  8. US
    Drugs & medicalClass II

    Remel, Inc recalls 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450

    Products may contain contamination, which may result in a darker or brown media color.

    FDA · DeviceRemel, IncWorldwide - US Nationwide distribution in the states of AK, CA, FL, GA, IA,…Official notice →
  9. 2025-08-06
  10. US
    Drugs & medicalClass II

    Remel, Inc recalls Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

    The products may contain surface and subsurface contamination of Listeria monocytogenes.

    FDA · DeviceRemel, IncUS Nationwide distribution.Official notice →
  11. 2025-06-18
  12. US
    Drugs & medicalClass II

    Remel, Inc recalls Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic…

    Product may have an off color affecting perfomance

    FDA · DeviceRemel, IncWorldwide - US Nationwide distribution in the states of AL, GA, KY, VA and the…Official notice →
  13. 2025-03-26
  14. US
    Drugs & medicalClass II

    Remel, Inc recalls Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ…

    Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.

    FDA · DeviceRemel, IncDomestic distribution to AL, AZ, CA, FL, GA, IN, KS, KY, MD, MI, NE, NY, OH,…Official notice →
  15. 2025-02-26
  16. US
    Drugs & medicalClass II

    Remel, Inc recalls remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

    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.

    FDA · DeviceRemel, IncUS Nationwide distribution.Official notice →
  17. 2024-11-06
  18. US
    Drugs & medicalClass II

    Remel, Inc recalls remel BactiDrop Acridine Orange, REF 21502, 50 per package.

    A color change of the solution within the dropper can occur from orange-yellow to light yellow resulting in out-of-specification fluorescent stain results.

    FDA · DeviceRemel, IncDistribution was made to IL, IN, MN, NE, SD, TX, VA, and WA. There was…Official notice →
  19. 2023-09-20
  20. US
    Drugs & medicalClass II

    Remel, Inc recalls remel TODD HEWITT W. CNA (LIM BROTH), REF R064810; used to isolate Group B Streptococci form clinical specimens containing mixed bacterial…

    On lot of Todd Hewitt Broth w/CNA (LIM) may exhibit no recovery of target organism during customer QC testing or use with patient samples

    FDA · DeviceRemel, IncUS Nationwide DistributionOfficial notice →
  21. 2023-07-05
  22. US
    Drugs & medicalClass II

    Remel, Inc recalls Remel Haemophilus Test Medium (Agar) (150mm), 10/pk, REF R04033; and Remel Haemophilus Test Medium (Agar)(100mm), 10/pk, REF 01503. For In…

    The test medium may not perform as intended.

    FDA · DeviceRemel, IncDistribution was made nationwide, including Puerto Rico. There was no foreign…Official notice →
  23. 2022-12-14
  24. US
    Drugs & medicalClass I

    Remel Inc recalls Thermo SCIENTIFIC, Sensititre STP6F, Gram Negative IVD AST

    An internal technical investigation has confirmed that Thermo Scientific" Gram Negative IVD AST Sensititre Plate may lead to false susceptible results for Proteae Tribe (including Proteus spp., Providencia spp.,…

    FDA · DeviceRemel IncUS Nationwide DistributionOfficial notice →
  25. 2022-03-16
  26. US
    Drugs & medicalClass II

    Remel Inc recalls Thermo Scientific Sensititre Gram Negative Susceptibility Testing Plate, IVD format

    There are lower than expected MICs for some gram negative species.

    FDA · DeviceRemel IncDistribution throughout the United States.Official notice →