Events

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 GE 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 037 01 11 000
  • Date de mise en oeuvre de l'événement
    2011-01-18
  • Pays de l'événement
    Saudi Arabia
  • Source de l'événement
    SFDA
  • URL de la source de l'événement
    https://ncmdr.sfda.gov.sa/Secure/CA/CaViewRecall.aspx?caid=5&rid=52
  • 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: http://www.sfda.gov.sa/En/MedicalEquipments/recalls/NCAR+Brief.htm
    SFDA urges all hospitals that have devices subjected to recall, to contact the company.
  • Cause
    Safety issue #1 the “view position” and laterality (e.G. lcc, rcc, lmlo, rmlo) is not displayed on mammography images on the web dx viewer. mammography images are expected to display view position and image laterality to support interpretation and diagnosis. the standard clinical practice is to verify laterality prior to mammographic‐based interventions or decisions. if the clinician does not verify correct laterality by an alternate means (e.G. by reviewing a correct hard copy, or by viewing the image on a mammography diagnostic workstation where the ‘view position’ and laterality are correctly displayed), then they could plan or perform an intervention or make diagnostic or treatment planning decisions on the wrong anatomic side or site. safety issue #2 image orientation or annotations are not displayed properly for an image on webdx viewer when displaying a ‘key image note’ that refers to multiple images with multiple presentation states. if a referring clinician relied exclusively on the ‘key image note’ for intervention or treatment decisions, and the annotations were essential for identifying or recognising the key finding, this could contribute to an incorrect or sub‐optimal intervention or treatment planning decision. details: the ‘key image note’ feature allows a radiologist to cue a referring clinician to critical findings/information based on selected key images. the ‘key image note’ can refer to multiple presentation states when it references more than one image in cases. examples of different presentation states that might be included in a ‘key image note’ include, but are not limited to: 1) images are not oriented in the same manner; 2) images do not have matching modality lut information’ 3) images do not have matching shutter information or graphic layer information. under these conditions, when a user opens the ‘key image note’ on a webdx viewer, the presentation state is not fully preserved. consequently, some image annotations are not displayed. safety issue #3 when a user is viewing a ’current’ exam and opens a ‘prior’ exam concurrently, the presentation display settings are not applied to the ‘prior’ exam. examples of presentation display settings include, but are not limited to, orientation markers, annotations and window levelling. this may result in image orientation, window level, invert, and annotations not being displayed as intended when an exam is displayed as a ‘prior’. this happens regardless of whether the exam is displayed as a ‘prior’ manually or via a hanging protocol. if a historical exam is opened independently (i.E. not while a ‘current’ exam is open), all presentation state and related annotation information is retained and correctly applied to the historic exam.

Device

GE Centricity PACS Web Diagnostic.
  • Modèle / numéro de série
    Software version: 1.0.0.x
  • Description du dispositif
    Picture archiving and communication system, radiology.
  • Manufacturer
    GE Healthcare.

Manufacturer

GE Healthcare.
  • Société-mère du fabricant (2017)
    General Electric Company
  • Représentant du fabricant
    GE Healthcare, Riyadh, (01) 4600530
  • Source
    SFDA