Cook Inc.: Medical Device Recall in 2018 - (Recall #: Z-0956-2018)

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:

Double Flexible Tipped Wire Guide

Product Classification:

Class II

Date Initiated: October 13, 2017

Date Posted: March 21, 2018

Recall Number: Z-0956-2018

Event ID: 79195

Reason for Recall:

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

Status: Terminated

Product Quantity: 10,367

Code Information:

Catalog # DTDW-/-BW Affected lots include: F3749839 - F4849938 NS5085893 - NS5827127 F4628078 - F4856722 3763189 - 6106860 F3739663 - F4916737 NS4980257 - NS6098990

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated