Microbiologics Inc: Device Recall

Recall #Z-2194-2025 · 06/27/2025

Class II: Risk

Recall Details

Recall Number: Z-2194-2025
Classification: Class II
Product Type: Device
Recalling Firm: Microbiologics Inc
Status: Ongoing
Date Initiated: 06/27/2025
Location: Saint Cloud, MN, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 32 units

Reason for Recall

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.

Product Description

LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894K (6-pack), 2) REF 0894P (2-pack)

Distribution Pattern

Worldwide distribution - US Nationwide and the countries of France, Colombia, Philippines, Peru, Turkey, India, Finland, Trinidad and Tobago, Poland, Viet Nam, Brazil, Japan, Malaysia, Costa Rica.

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 11/13/2025

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