Covidien LLC: Medical Device Recall in 2018 - (Recall #: Z-0908-2018)

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:

Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally invasive general abdominal, gynecologic and thoracic surgery for resection and transection of tissue and creation of anastomosis, as well as application deep in the pelvis, e.g. low anterior resection. They may be used for transection and resection of liver substance, hepatic vasculature and biliary structures and for transection and resection of pancreas.

Product Classification:

Class II

Date Initiated: September 15, 2017

Date Posted: March 14, 2018

Recall Number: Z-0908-2018

Event ID: 79166

Reason for Recall:

The device cartridge disengaged during use due to manufacturing error.

Status: Terminated

Product Quantity: 163

Code Information:

Product number: EGIARADXT Lot code: N6L0351X

Distribution Pattern:

Internationally, including Japan. No USA Customers

Voluntary or Mandated:

Voluntary: Firm initiated