Class II
Medical Device Recall: Campy CVA Medium 100/PK, R01272
Remel, Inc · February 5, 2026
Reason for Recall
Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium.
Distribution
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.
States Affected
NATIONWIDE
Quantity Affected
97
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1474-2026
Status: ongoing
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