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