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Ventana Medical Systems Inc recalls Ventana HE 600 System, automated slide preparer, for use in laboratories.
Recalled July 20, 2022 · FDA recall Z-1374-2022 · Ventana Medical Systems
Hazard
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire · FDA Class II
Units
763 instruments
Sold at
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Description
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
Product
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Manufacturer(s)
Ventana Medical Systems Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →