FDA Adverse Event
Death
Summary report: N
BCI PULSE PATIENT CABLE
MDR report key: 431911
·
Received December 4, 2002
Report
- Report Number
- 431911
- Event Type
- Death
- Date Received
- December 4, 2002
- Date of Event
- September 20, 2002
- Report Date
- November 20, 2002
- Manufacturer
- SIMS BCI, INC
- Product Code
- DSA
- Report Source
- User Facility report
- Reporter Location
- KY, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
WHEN A PERSON WENT INTO REPOSITION PT THEY FOUND PT WAS UNRESPONSIVE. THERE WAS NO INDICATOR LIGHT AT THE NURSES STATION, BUT ALARM WAS SOUNDING IN THE ROOM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | BCI PULSE PATIENT CABLE | MONITORING EXTENSION CABLE | DSA | SIMS BCI, INC | 3311 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Death |