Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There is a potential for fluid leak inside...
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
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Quantity: 763 instruments
Why Was This Recalled?
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
Where Was This Sold?
This product was distributed to 39 states: AL, AZ, AR, CA, CO, CT, FL, GA, HI, IL, IN, IA, KS, KY, MD, MA, MI, MN, MS, MO, MT, NE, NJ, NY, NC, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI, DC
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