Medical device recalls Moderate risk

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

Recall date
November 13, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0876-2026
FDA classification
Class II
Brand / firm
Microbiologics Inc
Sold / distributed
International distribution to the countries of UAE, China, Singapore, Kazakhstan,

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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