Campy CVA Medium 100/PK, R01272 recallZ-1474-2026 · Remel, Inc · initiated Feb 5, 2026
Open, Classified
Is my device affected?
- Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
- If yours is listed, follow the instructions from Remel, Inc or your healthcare provider. The company's action is summarized under what the company is doing.
- Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.
Where to find your model and lot numbers · What recall classes and statuses mean
Why it was recalled
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
FDA root cause category: Under Investigation by firm
What the company is doing
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.
Recall details
- Recall number
- Z-1474-2026
- Status
- Open, Classified
- Initiated by the company
- Feb 5, 2026
- Posted by the FDA
- Feb 26, 2026
- Recalling firm
- Remel, Inc
- Quantity
- 97
- Product code
- JSJ
- Distribution
- US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
Product description
Campy CVA Medium 100/PK, R01272
Code information (models, lots, serial numbers)
UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- REMEL R01272Remel, Inc. · Culture Media, Selective And Non-Differential1 recall0 reports
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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