Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal Recalled by Covidien, LP Due to Potential damage to the cartridge can result in...
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, LP directly.
Affected Products
Tri-Staple 2.0 Black Reinforced Intelligent Reload- Applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection of tissue and creation of anastomosis Model: SIGTRSB60AXT
Quantity: 1681 units
Why Was This Recalled?
Potential damage to the cartridge can result in poor staple formation and/or incomplete staple line, may cause a delay in surgery
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien, LP
Covidien, LP has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report