Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Recalled by COVIDIEN LLC Due to Sterilization method used was not consistent with 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 LLC directly.
Affected Products
Covidien Endo Grasp Auto Suture Grasper 5mm REF: 173030 The Covidien Endo Grasp" Auto Suture" grasper 5 mm instrument has applications in a variety of gynecologic, general, urologic, thoracic and endoscopic procedures for temporary grasping/clamping of tissue and small tubular structures.
Quantity: 240 units
Why Was This Recalled?
Sterilization method used was not consistent with the labeling and the approved sterilization method
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About COVIDIEN LLC
COVIDIEN LLC has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report