FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX

MDR report key: 2200821 · Received June 30, 2011

Report

Report Number
1218950-2011-01861
Event Type
Malfunction
Date Received
June 30, 2011
Report Date
June 1, 2011
Manufacturer
PHILIPS HEALTHCARE - ANDOVER
Product Code
MKJ
PMA / PMN Number
K031187
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CUSTOMER REPORTED THE DEVICE WOULD HANG OR LOCK UP IN POWER UP MODE. THE UNIT WAS EVALUATED AT PHILIPS AND THE SYMPTOM WAS VERIFIED. THE PROCESSOR PCA WAS REPLACED TO RESOLVE THE REPORTED ISSUE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THE DEVICE WOULD HANG OR LOCK UP IN POWER UP MODE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEARTSTART MRX MKJ PHILIPS HEALTHCARE - ANDOVER M3535A

Patients

Seq Age Sex Outcome Treatment
1