FDA Adverse Event Injury Summary report: N

MIDAS REX MRT PNEUMATIC HIGH SPEED SYSTEM

MDR report key: 5350729 · Received January 4, 2016

Report

Report Number
MW5059009
Event Type
Injury
Date Received
January 4, 2016
Date of Event
December 8, 2015
Report Date
December 31, 2015
Manufacturer
MEDTRONIC POWERED SURGICAL
Product Code
HBB
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
GA, US
Reporter Occupation
RISK MANAGER

Narratives

Description of Event or Problem · 1

MIDAS REX FOOTPLACE BROKE OFF DURING THE CRANIOTOMY FOR TUMOR. MIDAS REX LEGEND #8 IS THE SPECIFIC DRILL INVOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1908 MIDAS REX MRT PNEUMATIC HIGH SPEED SYSTEM MOTOR, DRILL, PNEUMATIC HBB MEDTRONIC POWERED SURGICAL MEDT T9850/C0375 A0279

Patients

Seq Age Sex Outcome Treatment
1 33 YR Required Intervention