Remel, Inc: Device Recall
Recall #Z-2224-2025 · 07/11/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2224-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Remel, Inc
- Status
- Ongoing
- Date Initiated
- 07/11/2025
- Location
- Lenexa, KS, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 371 units
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Product Description
Strep Selective II Agar, Product Number R01859
Distribution Pattern
US Nationwide distribution.
Other Recalls by Remel, Inc
- Class II: Risk 11/12/2025
- Class II: Risk 07/11/2025
- Class II: Risk 07/11/2025
- Class II: Risk 07/11/2025
- Class II: Risk 05/01/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.