Recall Z-1474-2026— Remel, Inc

Name: FDA recall Z-1474-2026
Creator: U.S. Food and Drug Administration
Published: 2026-02-05

Class II · Ongoing

Class II FDA medical device recall by Remel, Inc, initiated 2026-02-05. FDA's recall record names no specific 510(k) clearance for this event. Product: Campy CVA Medium 100/PK, R01272. Reason: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC 33291 on identified lot of medium..

Recalling firm: Remel, Inc
Classification: Class II
Status: Ongoing
Initiated: 2026-02-05
Firm location: Lenexa, KS, United States

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.