FDA Adverse Event
Malfunction
Summary report: N
LP6+ VOLUME VENTILATOR
MDR report key: 184966
·
Received August 25, 1998
Report
- Report Number
- 2183157-1998-00137
- Event Type
- Malfunction
- Date Received
- August 25, 1998
- Date of Event
- July 6, 1998
- Report Date
- August 25, 1998
- Manufacturer
- NELLCOR PURITAN BENNETT
- Product Code
- CBK
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
NELLCOR PURITAN BENNETT REC'D A CALL ON 07/06/1998. SOURCE CALLED TO REPORT THE FOLLOWING PROBLEM: INTERMITTENT STOP CYCLE ON INTERNAL BATTERY. NO PT HARM.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LP6+ VOLUME VENTILATOR | VOLUME VENTILATOR | CBK | NELLCOR PURITAN BENNETT | LP6+ | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |