Campy CVA Medium 100/PK recall (Remel, Inc)
Medical deviceClass IIOngoing
Summary: Remel, Inc is recalling Campy CVA Medium 100/PK, R01272. Reason: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
What is being recalled
Campy CVA Medium 100/PK, R01272
Why
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
How serious is it
Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.
Where it was sold
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA. (states named: Arizona, Colorado, Illinois, New Jersey, Ohio, Tennessee, Washington)
How to tell if yours is affected
UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
What to do
Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.
Recall facts
| Recall number | Z-1474-2026 |
| Category | Medical device |
| Agency | U.S. Food and Drug Administration (FDA) |
| Severity | Class II |
| Status | Ongoing |
| Recall started | February 5, 2026 |
| Reported | March 4, 2026 |
| Company | Remel, Inc |
| Company location | Lenexa, KS, United States |
| Initiated by | Voluntary: Firm initiated |
| Quantity | 97 |
More recalls from Remel, Inc · all medical device recalls · recalls from February 2026