Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ECHELON LINEAR Cutters Reload 80 mm Blue Recalled by Ethicon Endo-Surgery Inc Due to The devices were shipped unsterilized.
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
ECHELON LINEAR Cutters Reload 80 mm Blue, intended for transection, resection, and/or creation of anastomoses, Product Number GLC80
Quantity: 3 units
Why Was This Recalled?
The devices were shipped unsterilized.
Where Was This Sold?
International distribution to the countries of United Arab Emirates.
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