Events

Avis De Sécurité sur Vascular Guide Catheter, single-use

Selon Turkey Drugs and Medical Devices Agency (Titck), ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Turkey qui a été fabriqué par Boston Scientific.

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
    Field Safety Notice
  • ID de l'événement
    2016/891 & RA2016-124
  • Date
    2016-10-10
  • Pays de l'événement
    Turkey
  • Source de l'événement
    TDMDAT
  • URL de la source de l'événement
    https://web.archive.org/web/20170817142123/http://titck.gov.tr/PortalAdmin/Uploads/Titck/Dynamic/2016-891%20SGB.pdf
  • Notes / Alertes
    Turkish data is current through July 2017. All of the data comes from Turkey’s Drugs and Medical Devices Agency (Titck), 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 Turkey.
  • Notes supplémentaires dans les données

Device

Vascular Guide Catheter, single-use
  • Modèle / numéro de série
  • Description du dispositif
    Class III
  • Manufacturer
    Boston Scientific

Manufacturer

Boston Scientific
  • Société-mère du fabricant (2017)
    Boston Scientific
  • Commentaire du fabricant
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    TDMDAT