Remel, Inc: Device Recall
Recall #Z-2225-2025 · 07/11/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2225-2025
- 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
- 750 units
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Product Description
Blood/EMB, Levine 100/PK, Product Number R02041
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.