FDA Adverse Event Malfunction Summary report: N

HEARTSTART MRX

MDR report key: 3952169 · Received May 12, 2014

Report

Report Number
1218950-2014-02682
Event Type
Malfunction
Date Received
May 12, 2014
Report Date
April 17, 2014
Manufacturer
PHILIPS MEDICAL SYSTEMS
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). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED TO PHILIPS HEALTHCARE THAT THE CO2 CONNECTOR IS DISLODGED ON THE HEARTSTART MRX. THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
283899 HEARTSTART MRX MKJ PHILIPS MEDICAL SYSTEMS M3535A

Patients

Seq Age Sex Outcome Treatment
1