Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1886-2018 — 5mm Endopath Xcel with Optiview Technology, Bladeless Trocar with Stability Sleeve, 5mm, 75mm shaft length, 2B5ST

U.S. FDA — Device Enforcement · United States · 2018-03-26 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1886-2018
Date of alert
2018-03-26
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ethicon Endo-Surgery Inc
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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