FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX - EMS DEFIBRILLATOR

MDR report key: 3872575 · Received May 23, 2014

Report

Report Number
1218950-2014-02935
Event Type
Malfunction
Date Received
May 23, 2014
Report Date
May 2, 2014
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
MKJ
PMA / PMN Number
K031187
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

IT WAS REPORTED TO PHILIPS HEALTHCARE THAT THE HEARTSTART MRX HAD BROKEN BATTERY PINS. THERE IS NO REPORTED PATIENT INVOLVEMENT AND/OR IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
308991 HEARTSTART MRX - EMS DEFIBRILLATOR MKJ PHILIPS MEDICAL SYSTEMS M3536A

Patients

Seq Age Sex Outcome Treatment
1