FDA Adverse Event Injury Summary report: N

DRAEGER

MDR report key: 6793991 · Received August 11, 2017

Report

Report Number
MW5071561
Event Type
Injury
Date Received
August 11, 2017
Date of Event
July 31, 2017
Report Date
August 11, 2017
Manufacturer
DRAEGER, INC.
Product Code
CBK
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
AR, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

VENTILATOR SHUTDOWN WHILE ATTACHED TO PATIENT. PATIENT WAS DISCONNECTED AND O2 DELIVERED PER AMBU BAG UNTIL ANOTHER VENTILATOR WAS SET UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
569837 DRAEGER VENTILATOR CBK DRAEGER, INC. 500

Patients

Seq Age Sex Outcome Treatment
1 37 YR Life Threatening