Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Leica HistoCore SPECTRA CV Coverslipper Recalled by Leica Microsystems, Inc. Due to Product was assembled with an isolating fiberglass hose...
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
Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.
Quantity: 1 unit
Why Was This Recalled?
Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock.
Where Was This Sold?
This product was distributed to 1 state: MO
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