Nussloch GmbH ASP6025 Tissue Processor
Reported: July 12, 2017 Initiated: June 19, 2017 #Z-2660-2017
Product Description
Nussloch GmbH ASP6025 Tissue Processor
Reason for Recall
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
Details
- Recalling Firm
- Leica Microsystems, Inc.
- Units Affected
- 812 units
- 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.
- Location
- Buffalo Grove, IL
Frequently Asked Questions
What product was recalled? ▼
Nussloch GmbH ASP6025 Tissue Processor. Recalled by Leica Microsystems, Inc.. Units affected: 812 units.
Why was this product recalled? ▼
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 12, 2017. Severity: Moderate. Recall number: Z-2660-2017.
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