Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA Recalled by Covidien LLC Due to The device cartridge disengaged during use due to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Covidien LLC directly.
Affected Products
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.
Quantity: 163
Why Was This Recalled?
The device cartridge disengaged during use due to manufacturing error.
Where Was This Sold?
Internationally, including Japan. No USA Customers
About Covidien LLC
Covidien LLC has 248 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report