Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien TA Auto Suture Vascular Stapler with DST Series Technology Recalled by Covidien Llc Due to May contain a damaged internal component which could...
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
Covidien TA Auto Suture Vascular Stapler with DST Series Technology 30mm-V 3. Intended for abdominal, gynecological, pediatric and thoracic surgical procedures for resection or transection of tissue. Item Number: TA30V3S
Quantity: 3255 units US; 3574 units OUS
Why Was This Recalled?
May contain a damaged internal component which could impede staple deployment and result in incomplete staple formation and a non-functional staple line preventing adequate hemostasis, or leading to anastomotic leak, pneumothorax, tissue damage or other delayed secondary complications including infection, peritonitis, and sepsis
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien Llc
Covidien Llc has 59 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report