FDA Adverse Event Injury Summary report: N

DRAGER

MDR report key: 724221 · Received May 18, 2006

Report

Report Number
MW1039267
Event Type
Injury
Date Received
May 18, 2006
Date of Event
May 10, 2006
Report Date
May 18, 2006
Manufacturer
DRE, INC
Product Code
CBK
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

STAFF CALLED TO PT'S ROOM DUE TO SCREEN ON THE DRAGER VENT OUT. THE PT CONTINUED TO BE VENTILATED BY DRAGER MACHINE. THE SATURATIONS NEVER DROPPED BELOW 96%. THE PT HAD GOOD BILATERAL CHEST EXPANSION. PT NEVER IN ANY DISTRESS. DRAGER VENT SWITCHED OUT AND THE PT PLACED ON A NEW VENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DRAGER VENTILATOR CBK DRE, INC * *

Patients

Seq Age Sex Outcome Treatment
1 20 YR Disability