Z-1474-2026 Class II Ongoing
FDA device recall Z-1474-2026 was initiated by Remel, Inc on February 5, 2026 and is designated Class II. Reason for recall: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium. The recall status is ongoing. Affected quantity: 97.
Recall Details
- Product Type
- Devices
- Report Date
- March 4, 2026
- Initiation Date
- February 5, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 97
Product Description
Campy CVA Medium 100/PK, R01272
Reason for Recall
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Distribution Pattern
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
Code Information
UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026