KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802...

FDA Recall #Z-0876-2026 — Class II — November 13, 2025

Recall #Z-0876-2026 Date: November 13, 2025 Classification: Class II Status: Ongoing

Product Description

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.

Recalling Firm

Microbiologics Inc — Saint Cloud, MN

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

5 units

Distribution

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

Code Information

UDI-DI: 30845357020018; Lot Number: 818-111-7

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated