FDA recall Z-1474-2026

Remel, Inc · Class II · device

Product

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.

Distribution

US Nationwide distribution in the states of AZ, CO, IL, NJ, OH, TN, WA.

Key facts

Status
Ongoing
Initiation date
2026-02-05
Report date
2026-03-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lenexa, KS, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1474-2026