Z-2224-2025 Class II Ongoing
FDA device recall Z-2224-2025 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: 371 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
- 371 units
Product Description
Strep Selective II Agar, Product Number R01859
Reason for Recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Distribution Pattern
US Nationwide distribution.
Code Information
UDI-DI: 848838003158; Lot Numbers: 271613