RecallDepth

OptiView DAB IHC Detection Kit, Catalog Number 06396500001, model 760-700 Immunohistochemistry (IHC) for in vitro diagnostic use.

This recall has been terminated (originally issued September 14, 2018).

Company
Ventana Medical Systems Inc
Recall Initiated
August 2, 2018
Posted
September 14, 2018
Terminated
November 22, 2021
Recall Number
Z-2996-2018
Quantity
11,712 units
Firm Location
Oro Valley, AZ
Official Source
View on FDA website ↗

Reason for Recall

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

Distribution

worldwide

Lot / Code Info

Lot Numbers: Y25760, E00119, Y24225, UDI: 4015630984039

Root Cause

Under Investigation by firm

Action Taken

The firm disseminated their field safety notices by letter on 08/02/2018. The firm requested the destruction of the product.

More recalls by Ventana Medical Systems Inc

View all recalls by this company →