PlainRecalls
FDA Devices Critical Class I Terminated

CONFIRM anti-Progesterone Receptor (PR) (1E2) Rabbit Monoclonal Primary Antibody, Catalog Number 05278392001, model 790-4296 Immunohistochemistry (IHC) for in vitro diagnostic use.

Reported: September 26, 2018 Initiated: August 2, 2018 #Z-3006-2018

Product Description

CONFIRM anti-Progesterone Receptor (PR) (1E2) Rabbit Monoclonal Primary Antibody, Catalog Number 05278392001, model 790-4296 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
1655 units
Distribution
worldwide
Location
Oro Valley, AZ

Frequently Asked Questions

What product was recalled?
CONFIRM anti-Progesterone Receptor (PR) (1E2) Rabbit Monoclonal Primary Antibody, Catalog Number 05278392001, model 790-4296 Immunohistochemistry (IHC) for in vitro diagnostic use.. Recalled by Ventana Medical Systems Inc. Units affected: 1655 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-3006-2018.