Remel, Inc recalls Campy CVA Medium 100/PK
- Recalling company
- Remel, Inc
- Product
- Campy CVA Medium 100/PK, R01272
- Reason
- Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 5, 2026
- Reported
- Mar 4, 2026
- Distribution
- US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
- Status
- Ongoing
- Quantity
- 97
- Lot / codes
- UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
- Company location
- Lenexa, KS
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1474-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1474-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.