Cook Inc.: Medical Device Recall in 2018 - (Recall #: Z-0952-2018)

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:

Bentson Plus Wire Guide

Product Classification:

Class II

Date Initiated: October 13, 2017

Date Posted: March 21, 2018

Recall Number: Z-0952-2018

Event ID: 79195

Reason for Recall:

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

Status: Terminated

Product Quantity: 8,147

Code Information:

Catalog # TSFBP- / -BH Affected lots include: 3771080 - 5942053 F4265639

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated