Z-2223-2025 Class II Ongoing
FDA device recall Z-2223-2025 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: 1552 units.
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
- 1552 units
Product Description
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Distribution Pattern
US Nationwide distribution.
Code Information
UDI-DI: 848838000645; Lot Numbers: 271595, 271596