FDA Adverse Event
Malfunction
Summary report: N
LIFEPAK 12 DIFIBRILLATOR/MONITOR SERIES
MDR report key: 1000705
·
Received February 19, 2008
Report
- Report Number
- 3015876-2008-00069
- Event Type
- Malfunction
- Date Received
- February 19, 2008
- Report Date
- January 23, 2008
- Manufacturer
- PHYSIO-CONTROL, INC.
- Product Code
- LDD
- PMA / PMN Number
- K991910
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LIFEPAK 12 DIFIBRILLATOR/MONITOR SERIES | NONE | LDD | PHYSIO-CONTROL, INC. | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |