FDA Adverse Event Malfunction Summary report: N

SERVO VENTILATOR 300

MDR report key: 1140248 · Received June 19, 2008

Report

Report Number
1225700-2008-00089
Event Type
Malfunction
Date Received
June 19, 2008
Date of Event
June 12, 2008
Report Date
June 12, 2008
Manufacturer
MAQUET CRITICAL CARE AB
Product Code
CBK
Product Problem
Yes
Report Source
Distributor report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THAT THE VENTILATOR WAS NOT DELIVERING GAS WHILE IT WAS BEING CHECKED BY THE MEDICAL STAFF. THERE WAS NO PT CONNECTED TO THE VENTILATOR AT THE TIME OF THE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SERVO VENTILATOR 300 CBK CBK MAQUET CRITICAL CARE AB * *

Patients

Seq Age Sex Outcome Treatment
1 *