FDA Adverse Event Malfunction Summary report: N

MULTI DIAGNOST 4

MDR report key: 2102833 · Received April 12, 2011

Report

Report Number
3003768277-2011-00372
Event Type
Malfunction
Date Received
April 12, 2011
Report Date
April 12, 2011
Manufacturer
PHILIPS HEALTHCARE
Product Code
JAA
PMA / PMN Number
K961374
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE INVESTIGATION IS STILL ONGOING ON THIS EVENT. WHEN THE INVESTIGATION IS COMPLETED A F/U REPORT WILL BE SENT TO THE FDA.

Description of Event or Problem · 1

CUSTOMER REPORTED THAT IMAGES ON MONITOR ARE WASHED OUT. PICTURES CANNOT BE EVALUATED ANYMORE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MULTI DIAGNOST 4 JAA PHILIPS HEALTHCARE 708031

Patients

Seq Age Sex Outcome Treatment
1