# FDA recall Z-0308-2024

> **Microbiologics Inc** · Class II · device recall initiated 2023-10-18.

## Product

LYFO-DISK, P. venetum, Catalog number 0794L

## Reason for recall

A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.

## Distribution

Worldwide distribution - US Nationwide and the countries of Italy, France, Turkey, Peru, Mexico.

## Key facts

- **Recall number:** Z-0308-2024
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-10-18
- **Report date:** 2023-11-22

- **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-0308-2024

## Citation

> AI Analytics. FDA recall Z-0308-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0308-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
