Z-2226-2025 Class II Ongoing
FDA device recall Z-2226-2025 was initiated by Remel, Inc on July 11, 2025 and is designated Class II. Reason for recall: The products may contain surface and subsurface contamination of Listeria monocytogenes. The recall status is ongoing. Affected quantity: 611 untis.
Recall Details
- Product Type
- Devices
- Report Date
- August 6, 2025
- Initiation Date
- July 11, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 611 untis
Product Description
Blood/MacConkey Biplate 100/PK, Product Number R02049
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Distribution Pattern
US Nationwide distribution.
Code Information
UDI-DI: 848838003684; Lot Numbers: 274194