Class II

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

Microbiologics Inc · November 13, 2025

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,

Quantity Affected

5 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0876-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Microbiologics Inc Medical Device Recall: KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K | SafeCheck