Home / Recalls / Medical Devices
Medacta Usa recalls The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.
Recalled November 26, 2014 · FDA recall Z-0225-2015 · Medacta Usa
Hazard
The MectaLIF Oblique Handle has the laser marking "MEDIAL" on the incorrect side and could result in incorrect insertion of the device during surgery. · FDA Class II
Units
32 oblique handles
Sold at
Worldwide Distribution - US including CA, CO, ID and Internationally to Australia and Germany.
Description
The MectaLIF Oblique Handle has the laser marking "MEDIAL" on the incorrect side and could result in incorrect insertion of the device during surgery.
Product
The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.
Manufacturer(s)
Medacta Usa
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →