FDA DevicesClass II
Campy CVA Medium 100/PK, R01272
Published: March 4, 2026Recall ID: Z-1474-2026Category: devicesCountry: US
Reason for Recall / Hazard
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Product Description & Identification
Campy CVA Medium 100/PK, R01272
Additional Source Details
| Field | Value |
|---|---|
| City | Lenexa |
| State | KS |
| Event id | 98403 |
| Address 1 | 12076 Santa Fe Trail Dr |
| Address 2 | N/A |
| Code info | UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026 |
| Postal code | 66215-3519 |
| Report date | 20260304 |
| Product type | Devices |
| Product quantity | 97 |
| Reason for recall | Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium. |
| Voluntary mandated | Voluntary: Firm initiated |
| Recall initiation date | 20260205 |
| Initial firm notification | Letter |
| Center classification date | 20260226 |
Overview
- Recalling FirmRemel, Inc
- StatusOngoing
- Risk LevelClass II
- DistributionUS Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.