Ethicon Endo-Surgery Inc recalls Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM

Recalled June 7, 2017 · FDA recall Z-2174-2017 · Ethicon Endo-Surgery

Hazard

There is a risk that the pinion gear in the device could fail under extreme use cases. · FDA Class II

Units

792 units

Sold at

Worldwide distribution. The previously recalled products were distributed to the following countries: China, Japan, Singapore, and South Korea.

Description

There is a risk that the pinion gear in the device could fail under extreme use cases.

Product

Endopath ETS-FLEX Endoscopic Articulating Linear Cutter, VASCULAR/THIN 35MM

Manufacturer(s)

Ethicon Endo-Surgery Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →