FDA Adverse Event
Malfunction
Summary report: N
MIDAS REX I MO
MDR report key: 323860
·
Received March 1, 2001
Report
- Report Number
- 1625507-2001-00609
- Event Type
- Malfunction
- Date Received
- March 1, 2001
- Report Date
- October 28, 2000
- Manufacturer
- MEDTRONIC MIDAS REX
- Product Code
- HBB
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
"HOSE HAS LEAK" IS STATED ON THE REPAIR RECORDS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 8893 | MIDAS REX I MO | PNEUMATIC SURGICAL DRILL | HBB | MEDTRONIC MIDAS REX | N/A | N/A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |