PlainRecalls
FDA Devices Critical Class I Terminated

VENTANA anti-Helicobacter Pylori (SP48) PAB 250, Catalog Number 06425623001, model 790-1015 Immunohistochemistry (IHC) for in vitro diagnostic use.

Reported: September 26, 2018 Initiated: August 2, 2018 #Z-3010-2018

Product Description

VENTANA anti-Helicobacter Pylori (SP48) PAB 250, Catalog Number 06425623001, model 790-1015 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
2753 units
Distribution
worldwide
Location
Oro Valley, AZ

Frequently Asked Questions

What product was recalled?
VENTANA anti-Helicobacter Pylori (SP48) PAB 250, Catalog Number 06425623001, model 790-1015 Immunohistochemistry (IHC) for in vitro diagnostic use.. Recalled by Ventana Medical Systems Inc. Units affected: 2753 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-3010-2018.