Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Remel, Inc or your healthcare provider for instructions. Notification method: Letter
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Campy CVA Medium is used in laboratories for the testing of Campylobacter Jejuni, a bacteria causing gastrointestinal illness. Laboratories purchase this medium to ensure accurate testing results.
The identified lot of medium has shown low to no recovery of the bacteria, which compromises the reliability of test results and can lead to misdiagnosis.
This recall is not part of a broader industry pattern.
Patients and healthcare providers relying on this medium may face delays in accurate testing, potentially impacting patient care.
The lot number and expiration date can typically be found on the product label or packaging.
Expect a timeline of 4-8 weeks for any refunds or replacements associated with the recall.
Keep copies of any receipts, correspondence, and photographs of the product for your records.
The recalled product is Campy CVA Medium, with model UDI-DI 848838001055 and lot number R01272. It has an expiration date of January 12, 2026. The product was distributed nationwide in states including AZ, CO, IL, NJ, OH, TN, and WA.
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