FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 4791390 · Received May 22, 2015

Report

Report Number
1218950-2015-02785
Event Type
Malfunction
Date Received
May 22, 2015
Report Date
May 10, 2015
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

.

Description of Event or Problem · 1

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
334781 HEART START XL DEFIBRILLATOR MKJ PHILIPS MEDICAL SYSTEMS M4735A

Patients

Seq Age Sex Outcome Treatment
1