FDA Adverse Event
Malfunction
Summary report: N
LIFEPAK 7 DEFIBRILLATOR/MONITOR
MDR report key: 1082135
·
Received July 25, 2008
Report
- Report Number
- 3015876-2008-00837
- Event Type
- Malfunction
- Date Received
- July 25, 2008
- Date of Event
- May 1, 2008
- Report Date
- May 1, 2008
- Manufacturer
- PHYSIO-CONTROL, INC.
- Product Code
- MKJ
- PMA / PMN Number
- K810154
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
PARTS AND SVC FOR THIS DEVICE ARE NO LONGER SUPPORTED BY PHYSIO-CONTROL.
Description of Event or Problem · 1
ACCORDING TO THE RPTR, THE DEFIBRILLATOR WILL NOT CHARGE. THERE WAS NO PT ASSOCIATED WITH THE REPORT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LIFEPAK 7 DEFIBRILLATOR/MONITOR | MKJ | PHYSIO-CONTROL, INC. | 7 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |