FDAJune 3, 2021device

ECHELON FLEX Powered Plus Stapler-intended for transection, resection, and/or creation of anastomoses. The instruments have application in multiple open or minimally invasive general, gynecologic, urologic, thoracic, and pediatric surgical procedures. Product Code: PSEE60A

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Mislabeled: Labeled on the package as 60mm contains 45mm devices

What to do

FDA enforcement status: Terminated

Brands named

ethicon endo surgeryethiconethicon endo

UPCs

10705036014607

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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