Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endopath ETS-FLEX Endoscopic Articulating Linear Cutter Recalled by Ethicon Endo-Surgery Inc Due to There is a risk that the pinion gear...
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 ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM
Quantity: 792 units
Why Was This Recalled?
There is a risk that the pinion gear in the device could fail under extreme use cases.
Where Was This Sold?
Worldwide distribution. The previously recalled products were distributed to the following countries: China, Japan, Singapore, and South Korea.
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