Campy CVA Medium 100/PK, R01272
FDA device recall Z-1474-2026 · posted 2026-02-26 · Open, Classified
Recall details
- Recalling firm
- Remel, Inc
- Reason for recall
- Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
- Action taken
- On February 5, 2026, the firm notified affected customers via Urgent Medical Device Recall letter. Customers were instructed to review test results and destroy any remaining inventory of the affected lot.
- Root cause
- Under Investigation by firm
- Status
- Open, Classified
- Product code
- JSJ
- Quantity affected
- 97
- Distribution
- US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
- Date initiated
- 2026-02-05
- Date posted
- 2026-02-26
- Location
- Lenexa, KS
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