# FDA recall Z-0698-2022

> **Microbiologics Inc** · Class II · device recall initiated 2017-06-06.

## Product

Microbiologics QC Sets and Panels.  BD MAX" CT/GC/TV Verification and Control Panel.  Containing High, Medium and Low Level Controls.

## Reason for recall

Real-time shelf life testing failed at 24 months

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AK, CA, DC, FL, IA, ID, KS, LA, MD, MN, MO, NE, NH, NJ, NY, OH, OK, PA, SC, TX, VA, WA, WV and the countries of Australia, Belgium, Canada, India, United Kingdom.

## Key facts

- **Recall number:** Z-0698-2022
- **Recalling firm:** Microbiologics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-06
- **Report date:** 2022-03-09
- **Termination date:** 2023-01-17

- **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-0698-2022

## Citation

> AI Analytics. FDA recall Z-0698-2022. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0698-2022. Source: US FDA. Licensed CC0.

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