Campy CVA Medium 100/PK, R01272
FDA Recall #Z-1474-2026 — Class II — February 5, 2026
Product Description
Campy CVA Medium 100/PK, R01272
Reason for Recall
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Recalling Firm
Remel, Inc — Lenexa, KS
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
97
Distribution
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
Code Information
UDI-DI 848838001055 Lot R01272 lot 339135 Expired January 12, 2026
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated