Campy CVA Medium 100/PK — Class II medical device recall Z-1474-2026
Ongoing recall by Remel, Inc, reported 2026-03-04, distributed nationwide. Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
| Recall number | Z-1474-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel, Inc, Lenexa, KS, United States |
| Recall initiated | 2026-02-05 |
| Classified | 2026-02-26 |
| Reported by FDA | 2026-03-04 |
| Distributed | Nationwide (US) |
| Quantity | 97 |
| UPC / GTIN / UDI-DI | 00848838001055 |
| Lot numbers | 339135, R01272 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1474-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.