Microbiologics Inc: Device Recall

Recall #Z-0876-2026 · 11/13/2025

Class II: Risk

Recall Details

Recall Number: Z-0876-2026
Classification: Class II
Product Type: Device
Recalling Firm: Microbiologics Inc
Status: Ongoing
Date Initiated: 11/13/2025
Location: Saint Cloud, MN, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 5 units

Reason for Recall

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

Product Description

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

Distribution Pattern

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

Other Recalls by Microbiologics Inc

Class II: Risk 12/02/2025

Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Class II: Risk 12/02/2025

Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Class II: Risk 12/02/2025

Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Class II: Risk 06/27/2025

KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.
Class II: Risk 06/27/2025

KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.

View all recalls by Microbiologics Inc →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.