# FDA recall Z-2194-2025

> **Microbiologics Inc** · Class II · device recall initiated 2025-06-27.

## Product

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

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-2194-2025
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-27
- **Report date:** 2025-08-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Cloud, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2194-2025

## Citation

> AI Analytics. FDA recall Z-2194-2025. Retrieved 2026-07-08 from https://api.ai-analytics.org/recall/Z-2194-2025. Source: US FDA. Licensed CC0.

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