FDA Adverse Event
Other
Summary report: N
CAIRE
MDR report key: 150090
·
Received February 17, 1998
Report
- Report Number
- 2938572-1998-00001
- Event Type
- Other
- Date Received
- February 17, 1998
- Date of Event
- January 19, 1998
- Report Date
- January 30, 1998
- Manufacturer
- CAIRE INC
- Product Code
- CAW
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Distributor report
- Reporter Location
- FL, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
THE PORTABLE LIQUID UNIT BEGAN SHOOTING LIQUID OXYGEN THROUGH THE TOP OF THE UNIT AND THROUGH THE NASAL CANNULA DURING NORMAL USE AND IN THE UPRIGHT POSITION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | CAIRE | LIQUID OXYGEN PORTABLE | CAW | CAIRE INC | 1 & 2 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 56 YR | Other |