Cook Inc.: Medical Device Recall in 2018 - (Recall #: Z-0831-2018)

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:

Percutaneous Gastrojejunostomy Set Product Usage: Intended for the percutaneous placement of a catheter for gastroenteric feeding

Product Classification:

Class II

Date Initiated: October 19, 2017

Date Posted: March 7, 2018

Recall Number: Z-0831-2018

Event ID: 79192

Reason for Recall:

Cook has identified that the affected lots may contain wire guides that were loaded backwards into the wire guide holder.

Status: Terminated

Product Quantity: Quantities co-mingled into line 1

Code Information:

WOGS-1200-WH- 050493 Lot number: NS7587941

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated