Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aperio ScanScope System. Aperio ScanScope Models Recalled by Aperio Technologies Inc Due to Aperio initiated this recall because the User Guides...
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 Aperio Technologies Inc directly.
Affected Products
Aperio ScanScope System. Aperio ScanScope Models, XT, AT, AT Turbo, CS and CSO. Automated digital slide creation and viewing device. It is intended to create and view electronic image files representative of tissue specimens fixed to glass slides.
Quantity: 364
Why Was This Recalled?
Aperio initiated this recall because the User Guides incorrectly state the devices had been cleared for specific applications. The User Guides should state the devices are for Research Use Only and are not for use in diagnostic procedures.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aperio Technologies Inc
Aperio Technologies Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report