FDA Adverse Event
Other
Summary report: N
PROPAQ
MDR report key: 570740
·
Received January 14, 2005
Report
- Report Number
- 3023750-2005-00001
- Event Type
- Other
- Date Received
- January 14, 2005
- Report Date
- December 17, 2004
- Manufacturer
- WELCH ALLYN PROTOCOL, INC.
- Product Code
- DQA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
"MEMBER OF STAFF RECEIVED AN ELECTRIC SHOCK FROM THE UNIT, ATTEMPTING TO PLUG IN TRUNK LEAD INTO THE MONITOR. A BATTERY CHARGER WAS ALSO PLUGGED IN AT THE TIME."
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PROPAQ | CARDIAC MONITOR | DQA | WELCH ALLYN PROTOCOL, INC. | 206EL | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NO INFO | Other |