PlainRecalls
FDA Devices Critical Class I Terminated

ISH Protease 3, Catalog Number 05273331001, model 780-4149 Immunohistochemistry (IHC) for in vitro diagnostic use.

Reported: September 26, 2018 Initiated: August 2, 2018 #Z-3005-2018

Product Description

ISH Protease 3, Catalog Number 05273331001, model 780-4149 Immunohistochemistry (IHC) for in vitro diagnostic use.

Reason for Recall

Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.

Details

Units Affected
2231 units
Distribution
worldwide
Location
Oro Valley, AZ

Frequently Asked Questions

What product was recalled?
ISH Protease 3, Catalog Number 05273331001, model 780-4149 Immunohistochemistry (IHC) for in vitro diagnostic use.. Recalled by Ventana Medical Systems Inc. Units affected: 2231 units.
Why was this product recalled?
Leaking and sticking reagent dispensers for horseradish peroxidase (HRP) dispensers. A false negative IHC result may occur.
Which agency issued this recall?
This recall was issued by the FDA Devices on September 26, 2018. Severity: Critical. Recall number: Z-3005-2018.