FDA Adverse Event Injury Summary report: N

IMPACT INSTRUMENTATION INC

MDR report key: 480809 · Received August 28, 2003

Report

Report Number
480809
Event Type
Injury
Date Received
August 28, 2003
Date of Event
August 20, 2003
Report Date
August 22, 2003
Manufacturer
IMPACT INSTRUMENTATION
Product Code
CBK
Product Problem
Yes
Report Source
User Facility report
Reporter Location
LA, US
Reporter Occupation
PARAMEDIC

Narratives

Description of Event or Problem · 1

WHILE TRANSFERRING A PT FROM HOSPITAL TO HOSPITAL. PT WAS USING VENT. PT WAS TRANSFERRED TO STRETCHER. THE VENT THEN WENT INTO SYSTEM FAILURE. THE PT WAS IMMEDIATELY BAGGED THE REST OF TRIP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 IMPACT INSTRUMENTATION INC MODEL 754 EAGLE UNIVENT CBK IMPACT INSTRUMENTATION 754 *

Patients

Seq Age Sex Outcome Treatment
1 45 YR Life Threatening