# FDA recall Z-0784-2022

> **Microbiologics Inc** · Class II · device recall initiated 2022-02-25.

## Product

Mycoplasma genitalium Control Panel (Inactivated Pellet)

## Reason for recall

Distributed product did not undergo proper release testing.

## Distribution

Distribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA    OUS distribution to Belgium, Finland, France, Germany, Ireland, Sweden, United Kingdom, and Vietnam

## Key facts

- **Recall number:** Z-0784-2022
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-25
- **Report date:** 2022-03-23
- **Termination date:** 2024-01-16

- **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-0784-2022

## Citation

> AI Analytics. FDA recall Z-0784-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0784-2022. Source: US FDA. Licensed CC0.

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