Ventana Medical Systems Inc recalls Ventana HE 600 System, automated slide preparer, for use in
Recalled Product
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Hazard / Issue
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
Issued by
FDA
Affected States: AL, AR, AZ, CA, CO, CT, DC, FL, GA, HI, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV
Lot/Code Info: All Lots; UDI/DI: 04015630976010
View official government recall
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