Cook Inc.: Medical Device Recall in 2018 - (Recall #: Z-0966-2018)

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:

Femoral Artery Pressure Monitoring Set

Product Classification:

Class II

Date Initiated: October 13, 2017

Date Posted: March 21, 2018

Recall Number: Z-0966-2018

Event ID: 79195

Reason for Recall:

Label does not state that the product is heparin-coated.

Status: Terminated

Product Quantity: 266

Code Information:

Catalog # C-PMS-300-CHILDRENS-A- 032988 ALL LOTS

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated