FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX

MDR report key: 3983468 · Received June 27, 2014

Report

Report Number
1218950-2014-03720
Event Type
Malfunction
Date Received
June 27, 2014
Report Date
June 6, 2014
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
MKJ
PMA / PMN Number
K031187
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THEIR AC POWER MODULE IS MAKING A BUZZING SOUND. THERE WAS NO REPORTED PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
377094 HEARTSTART MRX MKJ PHILIPS MEDICAL SYSTEMS M3535A

Patients

Seq Age Sex Outcome Treatment
1