FDA Adverse Event
Death
Summary report: N
PLV 100
MDR report key: 248909
·
Received October 28, 1999
Report
- Report Number
- 248909
- Event Type
- Death
- Date Received
- October 28, 1999
- Date of Event
- August 8, 1999
- Manufacturer
- PLV
- Product Code
- CBK
- Report Source
- User Facility report
- Reporter Location
- VA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
PT FOUND DISCONNECTED FROM VENT. LOW PRESSURE ALARM DID NOT SOUND. DESCRIPITON OF DISCONNECTION: THE INNER CANNULA WAS PARTIALLY DISLODGED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PLV 100 | HOME CARE VENTILATOR | CBK | PLV | 100 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Death |