Reported Jul 20, 2022 · Ongoing
Ventana HE 600 System, automated slide preparer, for use in laboratories.
Ventana Medical Systems Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Ventana Medical Systems Inc · 1910 E Innovation Park Dr · Oro Valley, AZ · 85755-1962
Is this the product you have?
- Ventana HE 600 System, automated slide preparer, for use in laboratories.
- Lot codes and dates
- All Lots
- UDI/DI04015630976010
- Amount recalled
- 763 instruments
Where it was sold
Why it was recalled
There is a potential for fluid leak inside the Ventana HE 600 instrument which could result in electrical short and fire
This product could cause temporary or reversible health problems — stop using it.
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