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

Read the official notice →
Date
2025-06-18
Country
United States
Brand
Remel
Product
Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth w/ TES w/ Lysed Horse Blood, REF CP11410; invitro diagnostic…
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AL, GA, KY, VA and the…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Remel recalls

  1. 2026-03-04
  2. 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 →
  3. 2025-12-03
  4. 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 →
  5. 2025-08-06
  6. 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 →
  7. 2025-03-26
  8. 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 →
  9. 2025-02-26
  10. 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 →
  11. 2024-11-06
  12. 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 →
All 13 Remel recalls →

Other drugs & medical recalls in the United States

  1. 2025-06-18
  2. US
    Drugs & medicalClass II

    Contamac Solutions, Inc. recalls Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution

    Contact lens insertion solution may lack sterility.

    FDA · DeviceContamac Solutions, Inc.US Nationwide distribution in the states of AZ, CA, CO, FL, IL, IN, KS, KY,…Official notice →
  3. US
    Drugs & medicalClass II

    Tecfen Medical recalls Brand Name: Tecfen Medical Product Name: 3.2mm Slit Knife, Angled Model/Catalog Number: QKN3261 Software Version: No software Product…

    Sterility assurance for Ophthalmic knives.

    FDA · DeviceTecfen MedicalWorldwide - US Nationwide distribution in the states of Connecticut and…Official notice →
  4. US
    Drugs & medicalClass II

    Ortho-Clinical Diagnostics, Inc. recalls Brand Name: Solana¿ Bordetella Complete Assay Product Name: Solana Bordetella kit Model/Catalog Number: M308 Software Version:…

    It was determined that there could be a false positive rate of up to 16.7% for the affected lots associated with the Bordetella parapertussis (BPP) results (only) of the assay.

    FDA · DeviceOrtho-Clinical Diagnostics, Inc.Please see the attached list "Consignee List_CL2025-120." Note: This file…Official notice →
  5. US
    Drugs & medicalClass II

    Stryker GmbH recalls Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.

    Investigation determined that one lot of the T2 Greater Trochanter Nail (GTN) was labeled as left version but contained a right nail and another lot was labeled as right version but contained a left nail.

    FDA · DeviceStryker GmbHWorldwide - US Nationwide distribution in the states of California and…Official notice →
  6. US
    Drugs & medicalClass II

    GE Medical Systems Information Technologies Inc recalls MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer…

    The MUSE Administrator Account active directory or local credential could potentially be used from your local network to log into a GE HealthCare MUSE 5 system and potentially manipulate recorded patient data.

    FDA · DeviceGE Medical Systems Information Technologies IncWorldwide - US Nationwide distribution.Official notice →
  7. US
    Drugs & medicalClass II

    Copan Italia recalls BD BBL CultureSwab EZ Collection and Transport System, REF 220144, in vitro Diagnostic, SterileR, Rx Only

    Swabs for specimen collection may be prone to breakage during product usage.

    FDA · DeviceCopan ItaliaUS Nationwide distribution in the state of MD.Official notice →
See all drugs & medical recalls →