translation missing: fr.activerecord.attributes.event.titles.recall_field_safety_notice

Selon Saudi Food & Drug Authority, ce/cet/cette translation missing: fr.activerecord.attributes.event.types.recall_field_safety_notice concerne un dispositif en/au/aux/à Saudi Arabia qui a été fabriqué par Philips Healthcare.

Qu'est-ce que c'est?

Les avis de sécurité sont des communications que les fabricants de dispositifs médicaux ou leurs représentants font parvenir en particulier aux travailleurs du secteur médical, mais aussi aux utilisateurs de ces dispositifs. Les avis de sécurité concernent les actions entreprises quant aux dispositifs présents sur le marché et peuvent inclure des rappels et des alertes.

En savoir plus sur les données ici
  • Type d'événement
    Recall / Field Safety Notice
  • ID de l'événement
    mdprc 049 10 17 000
  • Date de mise en oeuvre de l'événement
  • Pays de l'événement
  • Source de l'événement
  • URL de la source de l'événement
  • Notes / Alertes
    Saudi data is current through January 2019. All of the data comes from the Saudi Food & Drug Authority, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Saudi Arabia.
  • Notes supplémentaires dans les données
    Report Source: NCMDR
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Cause
    Issue 1: cardiac signal not found in workflow issue if the operator loads a cardiac exam card, the cardiac signal is shown during cardiac scan but not shown during the surview. issue 2: scan may start at the top of the head, which may not be where the operator is expecting the scan to start if the operator plans to do multiple scans with multiple results including identical links then the first result of the subsequent acquisition will follow the last result of previous acquisition and not the identical link of the previous acquisition. the possible outcome is that the results of the second scan could be planned outside the boundaries of the expected results. issue 3: pulmo gates on cardiac workflow issue if the operator loads a cardiac exam card after performing a pulmonary scan, the pulmo wave may be present. ‘ issue 4: in the plan viewer if the start position is modified the total length of the acquisition will changes as well. in the plan viewer if the start position is modified by the length of one slice thickness, then the total length of the acquisition may change by the same length value as well. note this occurs only when planning without a surview. issue 5: image volumes are not found in patient directory when thin images are included in one of the multiple results the operator completes a ct orbit procedure and clicks end study’. the final thin images may not appear in patient directory. when the operator clicks ‘recon’ to attempt to do an off-line recon the ‘view 2 application may fail. issue 6: application may fail when modifying the results plan box during 3d calcium score while setting up a 3d calcium score scan, if the operator attempts to modify the plan box of a result on the surview, the application may fail and require a restart. issue 7; tube too hot the operator presses go’ to execute a timed scan sequence and the following message may display: “tube too hot”. issue 8: memory overflow issue when performing a ct clinical procedure, it is possible that the scan may be aborted as a result of a memory overflow issue. issue 9: while the reconstruction is in progress disconnecting the recon box (cirs) may not give error message when the connection between host computer and recon box (cirs) is disrupted during reconstruction, the operator may not be informed and may require that the operator reconstruct the images through off-line reconstruction. issue 10: issue with the generatormonitor state machine in rhost code issue when the operator turns the key switch on the ct box to off and turns it back on before the system gantry is turned off completely the system might make the generator to go into a configuration state and ceases to monitor and to send the updated real time data for the tube’s kv and ma.


  • Modèle / numéro de série
    Brilliance 64 728231 Ingenuity Core 728321 Ingenuity 1C2or8e 728323 Ingenuity CT 728326 : Running software version: 4.1,6 The products affected will display one of the following software versions: V4.1 .6.XXOSO V4.1 .6.XX032
  • Description du dispositif
    Computed Tomography
  • Manufacturer


  • Société-mère du fabricant (2017)
  • Représentant du fabricant
    Al-Faisaliah Medical System, Riyadh, (01) 2119948
  • Source