Remel, Inc recalls Campy CVA Medium 100/PK

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

On February 5, 2026, the firm notified affected customers via Urgent Medical Device Recall letter. Customers were instructed to review test results and destroy any remaining inventory of the affected lot.

• FDA enforcement recordOfficial FDA database entry for Z-1474-2026
• FDA device classification · JSJOfficial FDA classification for this device type
• CFR regulation · 21 CFR 866.2360The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Remel, IncSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.