medical MODERATE Updated 2026-03-04

Remel, Inc recalls Campy CVA Medium 100/PK, R01272

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Recalled Product

Campy CVA Medium 100/PK, R01272

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Hazard / Issue

Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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