FDA Adverse Event
Malfunction
Summary report: N
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
MDR report key: 2923628
·
Received January 22, 2013
Report
- Report Number
- 1031452-2013-00126
- Event Type
- Malfunction
- Date Received
- January 22, 2013
- Report Date
- January 19, 2013
- Manufacturer
- INVACARE FLORIDA OPERATIONS
- Product Code
- CAW
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Description of Event or Problem · 1
DEALER STATES HE IS NOT CONFIDENT OF THE ACCURACY OF THE FLOWMETER WHEN ITS MEASURING FRACTIONAL OUTPUT. HE STATED HE SEES ALL MANUFACTURED FLOWMETERS ARE EQUAL IN THIS AREA.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 31128 | PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL) | 868.5440 | CAW | INVACARE FLORIDA OPERATIONS | IRCPF16 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |