FDA Adverse Event
Other
Summary report: N
AIRLIFE
MDR report key: 811223
·
Received January 30, 2007
Report
- Report Number
- MW1041805
- Event Type
- Other
- Date Received
- January 30, 2007
- Date of Event
- January 18, 2007
- Report Date
- January 30, 2007
- Manufacturer
- CARDINAL HEALTH
- Product Code
- CAT
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- OH, US
- Reporter Occupation
- BIOMEDICAL ENGINEER
Narratives
Description of Event or Problem · 1
THE PATIENT WAS SET UP ON A NASAL CANNULA. THE NASAL CANNULA WAS FAULTY. THE INSIDE OF THE CANNULA DID NOT HAVE AN OPEN LUMEN. IT WAS OCCLUDED AND COULD NOT DELIVER THE PRESCRIBED OXYGEN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | AIRLIFE | NASAL CANNULA | CAT | CARDINAL HEALTH | UNAVAILABLE | UNAVAILABLE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 43 YR | Other |