Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by Ventana Medical Systems Inc Due to Ventana Medical System is initiating the recall of...
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 Ventana Medical Systems Inc directly.
Affected Products
Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS, N750-BMKXT-FS, N750-BMKLT-FS, N750-DIS-FS, N750-DISXT-FS. Product Usage: Usage: The Benchmark product lines are intended to automatically stain histological or cytological specimens on microscope slides with specific immunohistochemistry or in situ hybridization reagents for in vitro diagnostic use. The Discovery Systems are research use only instruments with similar functionality.
Quantity: 1217 units total
Why Was This Recalled?
Ventana Medical System is initiating the recall of the BenchMark and DISCOVERY series instruments because there is a possibility that the heating element could separate from the underside of the heater cap and cause a non-staining or inconsistent staining event. Additionally, the system may not detect this anomaly and therefore it may not generate an error message for the slide position.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ventana Medical Systems Inc
Ventana Medical Systems Inc has 39 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report