Ethicon Endo-Surgery Inc recalls Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VAS
See all recalls from Ethicon Endo-Surgery Inc →Recalled Product
Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM
Hazard / Issue
There is a risk that the pinion gear in the device could fail under extreme use cases.
Issued by
FDA
Distribution: Worldwide distribution. The previously recalled products were distributed to the following countries: China, Japan, Singapore, and South Korea.
Lot/Code Info: N91U0W, N91U0X, N91L2P, N91N1J, and N91N2G
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Endopath ETS-FLEX Endoscopic Articulating →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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