Home / Recalls / Medical Devices
COVIDIEN MEDTRONIC recalls Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product
Recalled April 26, 2017 · FDA recall Z-1836-2017 · COVIDIEN MEDTRONIC
Hazard
Customer reports of the device handset continuing to operate after release of the activation button. · FDA Class II
Units
24,703 Units
Sold at
Worldwide - US Nationwide Distribution in the states of: AR AZ CA CO FL GA IA IL KS KY LA MA MI MN MO MS NC NE NM NY OH OR PA SC SD TN TX VA WA WV
Description
Customer reports of the device handset continuing to operate after release of the activation button.
Product
Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannulas or larger cannulas with 5mm adapters during laparoscopic and thorascopic procedures. For use with a minimum peak voltage of 3625V.
Manufacturer(s)
COVIDIEN MEDTRONIC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →