Medical device recalls Moderate risk

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

Recall date
February 5, 2026
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1474-2026
FDA classification
Class II
Brand / firm
Remel, Inc
Sold / distributed
US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Campy CVA Medium 100/PK, R01272

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