# FDA recall Z-2660-2017

> **Leica Microsystems, Inc.** · Class II · device recall initiated 2017-06-19.

## Product

Nussloch GmbH ASP6025 Tissue Processor

## Reason for recall

Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.

## Distribution

Domestic: AR, AZ, CA, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MN, MO, MT, NC, NE, NJ, NM, NV, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI, WV, & DC. Foreign: Australia, Austria, Bangladesh, Belgium, Brazil, Canada, Chile, China, Colombia, Costa Rica, Czech Republic, England, France, Georgia, Germany, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Korea, Kuwait, Lithuania, Malaysia, Maldives, Mexico, Morocco, Myanmar, Netherlands, Norway, Peru, Philippines, Poland, Portugal, Qatar, Reunion, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovenia, South Africa, Spain, Switzerland, Taiwan, Thailand, Turkey, & United Arab Emirates.

## Key facts

- **Recall number:** Z-2660-2017
- **Recalling firm:** Leica Microsystems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2017-06-19
- **Report date:** 2017-07-12

- **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-2660-2017

## Citation

> AI Analytics. FDA recall Z-2660-2017. Retrieved 2026-07-19 from https://api.ai-analytics.org/recall/Z-2660-2017. Source: US FDA. Licensed CC0.

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