PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: December 10, 2025 Initiated: November 13, 2025 #Z-0876-2026

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.

Details

Recalling Firm
Microbiologics Inc
Units Affected
5 units
Distribution
International distribution to the countries of UAE, China, Singapore, Kazakhstan,
Location
Saint Cloud, MN

Frequently Asked Questions

What product was recalled?
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K. Recalled by Microbiologics Inc. Units affected: 5 units.
Why was this product recalled?
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 10, 2025. Severity: Moderate. Recall number: Z-0876-2026.