Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Best Practice Kits containing certain production lots of Endo GIA Recalled by Medtronic Due to Staplers fail to fire or partially fire and...
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 Medtronic directly.
Affected Products
Best Practice Kits containing certain production lots of Endo GIA Ultra Universal Stapler Handles Product Usage: The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and creation of anastomosis. It may be used for transection and resection of liver substance, hepatic vasculature and biliary structures. The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers when used with the Endo GIA curved tip single use reloads can be used to blunt dissect or separate target tissue from other tissue.
Quantity: 2711 kits
Why Was This Recalled?
Staplers fail to fire or partially fire and reports of the instrument articulating lever disengaging during use
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic
Medtronic has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report