Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Recalled by Leica Microsystems, Inc. Due to The Leica ASP200S/ASP300S Tissue Processor have an incorrect...
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
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue Processor is an automated system used to process tissue specimens for examination through fixation, dehydration and infiltration.
Quantity: 901
Why Was This Recalled?
The Leica ASP200S/ASP300S Tissue Processor have an incorrect internal wiring to the remote alarm plug, which can cause the remote alarm to not function correctly in the case of an instrument failure.
Where Was This Sold?
This product was distributed to 31 states: AZ, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KY, LA, MD, MA, MN, MO, MT, NJ, NM, NY, NC, OH, OR, PA, TX, VA, WA, WV, WI
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