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 |