FDA Device recall Z-1474-2026
Campy CVA Medium 100/PK, R01272
- FDA Device
- Class II
- ongoing
- Published 2026-03-04
On 2026-03-04 the FDA classified a Class II recall of Campy CVA Medium 100/PK, R01272 by Remel, citing customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1474-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-02-05 |
| Published | 2026-03-04 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Remel |
| Distribution | US |
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.
Identifiers
| code_info | UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1474-2026%22
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