# FDA recall Z-2399-2020

> **Leica Microsystems, Inc.** · Class II · device recall initiated 2020-05-20.

## Product

Leica ARveo and M530 OH6 microscope systems.

## Reason for recall

Possible unintended interruption of surgical procedures due to equipment shutdown, related to changes in voltage.

## Distribution

Domestic distribution: AL,AR,AZ, CA, CT, DC, DE, FL, IL, KY, LA, MI, MN, MO, NC, NY, OH. OR. TN, TX, UT, VA, WA, WI ,WV.  International distribution: Japan

## Key facts

- **Recall number:** Z-2399-2020
- **Recalling firm:** Leica Microsystems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-05-20
- **Report date:** 2020-06-24
- **Termination date:** 2021-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Buffalo Grove, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2399-2020

## Citation

> AI Analytics. FDA recall Z-2399-2020. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-2399-2020. Source: US FDA. Licensed CC0.

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