FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX- EMS DEFIBRILLATOR

MDR report key: 1070674 · Received July 1, 2008

Report

Report Number
1218950-2008-00352
Event Type
Malfunction
Date Received
July 1, 2008
Report Date
June 2, 2008
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
LDD
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE FACTORY HAS NOT YET RECEIVED THE DEVICE FOR EVALUATION, AND THIS COMPLAINT IS STILL UNDER INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THIS DEVICE HAS A SYNC BUTTON THAT IS STICKING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEARTSTART MRX- EMS DEFIBRILLATOR DEFIBRILLATOR LDD PHILIPS MEDICAL SYSTEMS M3536A

Patients

Seq Age Sex Outcome Treatment
1