# FDA recall Z-2659-2018

> **Leica Microsystems, Inc.** · Class II · device recall initiated 2018-06-25.

## Product

Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.

## Reason for recall

Recall is due to a design weakness of the power insert module.

## Distribution

United States distribution: AR, AZ, CA, CO, CT, DE, FL, IL, IN, KS, KY, LA, MO, NJ, NY,  NV, OH, OR, PA, TX, UT, PR.      International distribution to Japan, Brazil, Columbia, Ecuador, Mexico, Taiwan

## Key facts

- **Recall number:** Z-2659-2018
- **Recalling firm:** Leica Microsystems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-06-25
- **Report date:** 2018-08-15
- **Termination date:** 2019-02-26

- **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-2659-2018

## Citation

> AI Analytics. FDA recall Z-2659-2018. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-2659-2018. Source: US FDA. Licensed CC0.

---

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