FDA Adverse Event
Malfunction
Summary report: N
PHYSIO-CONTROL LIFEPAK 20
MDR report key: 1180263
·
Received September 19, 2008
Report
- Report Number
- 1180263
- Event Type
- Malfunction
- Date Received
- September 19, 2008
- Date of Event
- August 14, 2008
- Report Date
- September 19, 2008
- Manufacturer
- MEDTRONIC INC. (MEDTRONIC EMERGENCY RESPONSE SYSTEMS)
- Product Code
- LDD
- Product Problem
- Yes
- Report Source
- User Facility report
- Reporter Location
- WI, US
Narratives
Description of Event or Problem · 1
DEFIBRILLATOR FAILED TO CHARGE ON BATTERY POWER. WHEN PLUGGED INTO THE WALL, THE UNIT WORKED PROPERLY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PHYSIO-CONTROL LIFEPAK 20 | DEFIBRILLATOR | LDD | MEDTRONIC INC. (MEDTRONIC EMERGENCY RESPONSE SYSTEMS) | LIFEPAK 20 | 2003 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |