FDA recall record

Ethicon Endo-Surgery Endoscopic Articulating Linear Cutter, ATB35 recall — FDA Z-0295-2017

Quality control identified a component issue where the pinion gear in the device could fail under extreme use cases. If this condition occurs, staples…

Class IIclassification
Z-0295-2017official record ID
Oct 26, 2016report date

Recall record at a glance

Official recordZ-0295-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmEthicon Endo-Surgery Inc.
Report dateOct 26, 2016
Recall initiation dateJul 15, 2016
Quantity105
LocationBlue Ash, OH, United States

Official product description

Endoscopic Articulating Linear Cutter, ATB35. Standard 35 MM. The ENDOPATH ETS-Flex Endoscopic Articulating Linear Cutter has application in general, gynecologic, urologic, and thoracic surgery for transection, resection, and/or creation of anastomoses

Why the product was recalled

Quality control identified a component issue where the pinion gear in the device could fail under extreme use cases. If this condition occurs, staples will be formed past the cut line and the device can be opened and removed from the patient. The firing stroke may be interrupted and the knife may not fully return to the home position potentially exposing the healthcare professional to a sharps injury.

Distribution information

Worldwide Distribution - US including AL, AR, AZ, CA, CO,CT, DC, FL,GA, IA,IL,KS,KY,LA,MA,MD, ME, MI,MN,MO, MS, MT,NC, ND, NH,NJ, NM, NV, NY, OH, RI, TN, TX, VA, VT, WA, WI and Internationally to Brazil and Canada.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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About this record

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