FDA recall Z-0876-2026

Microbiologics Inc · Class II · device

Product

KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K

Reason for recall

Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.

Distribution

International distribution to the countries of UAE, China, Singapore, Kazakhstan,

Key facts

Status
Ongoing
Initiation date
2025-11-13
Report date
2025-12-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Saint Cloud, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0876-2026