FDA Adverse Event Malfunction Summary report: N

DIAGNOST 93

MDR report key: 2012202 · Received February 1, 2011

Report

Report Number
3003768277-2011-00091
Event Type
Malfunction
Date Received
February 1, 2011
Report Date
January 5, 2011
Manufacturer
PHILIPS HEALTHCARE
Product Code
JAA
PMA / PMN Number
K912470
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THIS EVENT IS STILL UNDER INVESTIGATION. THE FOLLOW-UP REPORT WILL BE SENT BY 04/03/2011.

Description of Event or Problem · 1

THE CUSTOMER STATES "DESPITE SERVICE, THE PROBLEM HAS RETURNED, THE FLUOROSCOPY HAS STOPPED AGAIN".

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DIAGNOST 93 JAA PHILIPS HEALTHCARE 70847

Patients

Seq Age Sex Outcome Treatment
1