Ventana Medical Systems Inc: Medical Device Recall in 2018 - (Recall #: Z-3001-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093. For laboratory use.

Product Classification:

Class I

Date Initiated: August 2, 2018

Date Posted: September 26, 2018

Recall Number: Z-3001-2018

Event ID: 80807

Reason for Recall:

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

Status: Terminated

Product Quantity: 10 units

Code Information:

Lot Number: Y19981, UDI: 4015630970261

Distribution Pattern:

worldwide

Voluntary or Mandated:

Voluntary: Firm initiated