FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 4801999 · Received May 28, 2015

Report

Report Number
1218950-2015-02876
Event Type
Malfunction
Date Received
May 28, 2015
Report Date
May 19, 2015
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TW
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT DEVICE CANNOT BOOT UP. THERE WAS NO REPORTED PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
346416 HEART START XL DEFIBRILLATOR MKJ PHILIPS MEDICAL SYSTEMS M4735A

Patients

Seq Age Sex Outcome Treatment
1