FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX -EMS DEFIBRILLATOR

MDR report key: 1062206 · Received June 13, 2008

Report

Report Number
1218950-2008-00322
Event Type
Malfunction
Date Received
June 13, 2008
Report Date
May 20, 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 EVAL, AND THIS COMPLAINT IS STILL UNDER INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED INTERMITTENT STICKING OF THE SYNC BUTTON.

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