Home / Recalls / Medical Devices
Leica Microsystems, Inc. recalls Nussloch GmbH ASP6025 Tissue Processor
Recalled July 12, 2017 · FDA recall Z-2660-2017 · Leica Microsystems
Hazard
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit. · FDA Class II
Units
812 units
Sold at
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.
Description
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
Product
Nussloch GmbH ASP6025 Tissue Processor
Manufacturer(s)
Leica Microsystems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →