Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip Recalled by Ethicon Endo-Surgery Inc Due to During an internal inspection of the production process...
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 Ethicon Endo-Surgery Inc directly.
Affected Products
ENDOPATH ECHELON" Vascular White Reload for Advanced Placement Tip, Product Usage: The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic and pediatric surgical procedures.
Quantity: 6,744 devices
Why Was This Recalled?
During an internal inspection of the production process the firm discovered an issue which may cause the cartridge to deploy an incomplete staple line.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Ethicon Endo-Surgery Inc
Ethicon Endo-Surgery Inc has 54 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report