FDA Medical devices recall ·
Campy CVA Medium 100/PK, R01272 recall
- Recall number
- Z-1474-2026
- Date
- (initiated February 5, 2026)
- Company / brand
- Remel, Inc
12076 Santa Fe Trail Dr, Lenexa, KS, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 97
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Campy CVA Medium 100/PK, R01272
Why was it recalled?
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
Distribution
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
States: Arizona Colorado Illinois New Jersey Ohio Tennessee Washington
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1474-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.