Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EGIA 60 ARTICULATING EXTRA THICK SULU Recalled by Covidien LLC Due to The device may be missing one of two...
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
EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT
Quantity: 3,113,280
Why Was This Recalled?
The device may be missing one of two pin components that maintain alignment of the device jaws, resulting in incomplete staple formation which may lead to bleeding, anastomotic leak, peritonitis, or pneumothorax which can result in the potential for infection and/or sepsis.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Covidien LLC
Covidien LLC has 248 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report