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Campy CVA Medium
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MEDICAL DEVICE RECALLMODERATE

Campy CVA Medium

Remel is recalling Campy CVA Medium (R01272) due to low recovery of Campylobacter Jejuni on identified lots.

What to do

Stop using affected lot(s) of Campy CVA Medium immediately. Contact Remel, Inc. for lot number verification and replacement product or refund. Do not use this medium for bacterial culture or diagnostic testing.

Recalled
Listed
Updated
Recall No.
Z-1474-2026
Agency
FDA
Firm
Remel, Inc
Recall ID
98403
Status
ONGOING

Why it was recalled

Remel, Inc. is recalling Campy CVA Medium 100/PK (Model R01272) due to low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot(s) of medium. The product is used for bacterial culture and recovery in clinical and research laboratories. Affected units were distributed nationwide to AZ, CO, IL, NJ, OH, TN, and WA.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Campy CVA Medium 100/PK, R01272

UDI-DI
848838001055

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification