FDAMarch 26, 2018device

5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 150mm shaft length, 2B5XT

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

The hazard

Use of the product with insufficient lubrication may prolong surgery due to trocar replacement. In addition, insufficient lubrication could result in a remote chance of introducing a minute particle if repeated insertions of the obturator or laparoscopic device damage the seal.

What to do

FDA enforcement status: Terminated

Brands named

ethicon endo surgeryethiconethicon endo

Recall history

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

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