Home / Recalls / Medical Devices
Neotract Inc recalls UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Recalled August 10, 2022 · FDA recall Z-1502-2022 · Neotract
Hazard
There is the potential that during implant deployment, the device may not properly deliver a implant. · FDA Class II
Units
18,722 systems
Sold at
US: AK AL AR AZ CA CO CT DC DE FL GA IA IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NY OH OK PA RI SC SD TN TX UT VA VT WI WV OUS: None
Description
There is the potential that during implant deployment, the device may not properly deliver a implant.
Product
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Manufacturer(s)
Neotract Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →