FDA Adverse Event
Death
Summary report: N
UNK
MDR report key: 41546
·
Received October 2, 1996
Report
- Report Number
- 2022906-1996-00005
- Event Type
- Death
- Date Received
- October 2, 1996
- Date of Event
- July 17, 1996
- Report Date
- October 2, 1996
- Manufacturer
- SPACELABS MED, INC.
- Product Code
- MHX
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- VA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
ALARMS ON BEDSIDE FOUND OFF AND PT HAD OXYGEN SATURATION OF 40%.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | UNK | BEDSIDE MONITOR | MHX | SPACELABS MED, INC. | 90303A | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 31 YR | Death |