Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling 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
Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling system 60 mm Extra Thick, Item Code SIG60AXT
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