Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nussloch GmbH ASP6025 Tissue Processor Recalled by Leica Microsystems, Inc. Due to Incorrect labeling for specified voltage for the Alarm...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Leica Microsystems, Inc. directly.
Affected Products
Nussloch GmbH ASP6025 Tissue Processor
Quantity: 812 units
Why Was This Recalled?
Incorrect labeling for specified voltage for the Alarm Connectors on the rear side of the unit.
Where Was This Sold?
This product was distributed to 36 states: AZ, AR, CA, CT, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, MD, MA, MN, MO, MT, NE, NV, NJ, NM, NY, NC, OH, PA, SC, TN, TX, UT, VA, WA, WV, WI, DC
About Leica Microsystems, Inc.
Leica Microsystems, Inc. has 40 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report