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