# FDA recall Z-1075-2024

> **Microbiologics Inc** · Class II · device recall initiated 2024-01-08.

## Product

Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.

## Reason for recall

The negative control was contaminated with one of the positive control pathogens (Norovirus).  This would result in users getting a positive call for Norovirus when running the negative control.

## Distribution

US Nationwide distribution in the states of AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, MA, MI, MN, MO, MS, MT, NE, NH, NJ, NY, OH, PA, RI, TN, TX, VA, WA, WI, WV, and WY.  There was government distribution and no military distribution.  Foreign distribution was made to France.

## Key facts

- **Recall number:** Z-1075-2024
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-01-08
- **Report date:** 2024-02-21

- **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-1075-2024

## Citation

> AI Analytics. FDA recall Z-1075-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1075-2024. Source: US FDA. Licensed CC0.

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