FDA Adverse Event
Other
Summary report: N
UNK
MDR report key: 455852
·
Received April 15, 2003
Report
- Report Number
- 455852
- Event Type
- Other
- Date Received
- April 15, 2003
- Date of Event
- March 20, 2003
- Report Date
- April 14, 2003
- Manufacturer
- UNK
- Product Code
- GZB
- Report Source
- User Facility report
- Reporter Location
- TX, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
ADD'L INFO RECEIVED FROM MFR 6/18/03: THE DEVICE REFERENCED IN THE ABOVE REPORT HAS NOT BEEN RETURNED TO MEDTRONIC INC, FOR EVLAUATION. REPEATED ATTEMPTS TO THE HEALTH CARE PROVIDED HAVE NOT PROVIDED ANY INFO RELATED TO WHY THE DEVICE WAS REMOVED.
Description of Event or Problem · 1
MEDTRONIC BATTERY REMOVED FROM STIMULATOR.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNK | UNK | GZB | UNK | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 51 YR | Other |