Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology Recalled by COVIDIEN MEDTRONIC Due to Device may be missing a sled component. The...
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 MEDTRONIC directly.
Affected Products
Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology, Item Code EGIA60AMT
Why Was This Recalled?
Device may be missing a sled component. The sled component is responsible for staple deployment. This may result in failure to form a staple line when tissue is divided, leading to bleeding or leakage of luminal contents.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About COVIDIEN MEDTRONIC
COVIDIEN MEDTRONIC has 55 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report