FDA Adverse Event
Injury
Summary report: N
WEST MED PEDI CO2 EASY
MDR report key: 1630798
·
Received March 10, 2010
Report
- Report Number
- MW5015100
- Event Type
- Injury
- Date Received
- March 10, 2010
- Date of Event
- January 16, 2010
- Report Date
- March 3, 2010
- Manufacturer
- WESTMED, INC.
- Product Code
- CCK
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
CARBON DIOXIDE DETECTOR IS TO CHANGE FROM PURPLE TO YELLOW ONCE AIRWAY - DETECTOR NEVER WENT TO YELLOW RATHER TO BEIGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | WEST MED PEDI CO2 EASY | PEDI CO2 DETECTOR | CCK | WESTMED, INC. | 562135 | 46058 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 2 DA | Life Threatening |