inforMED
MalfunctionIZF

PHILIPS INTEGRIS H

Received Dec 30, 2014 · Event occurred Oct 13, 2014

Report MW5039954 · MDR key 4387175

Device

Generic name

Xray System

Manufacturer

Philips

Model number

ERROR

Product problems

  • Loss of Data
  • Device Operates Differently Than Expected

Patient

63 YR

  • No Known Impact Or Consequence To Patient

Narrative

Description of Event or Problem

FILMS FROM BIVENTRICULAR PERMANENT PACEMAKER PLACEMENT AND ABLATION UNABLE TO BE SENT TO PERMANENT STORAGE. PHILIPS SERVICE REP EVALUATED EQUIPMENT AND FELT REASON FILMS WOULD NOT BE SENT WAS DUE TO THE CASE FILE BEING CORRUPT. FILMS HAD TO BE DELETED FROM EQUIPMENT. CATH LAB 7.