Events

Avis De Sécurité sur Optisure Dual Coil Defibrillation lead

Selon Swiss Agency for Therapeutic Products, ce/cet/cette avis de sécurité concerne un dispositif en/au/aux/à Switzerland qui a été fabriqué par St. Jude Medical.

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
    Vk_20151105_03
  • Date de publication de l'événement
    2015-11-16
  • Pays de l'événement
    Switzerland
  • Source de l'événement
    SATP
  • URL de la source de l'événement
    https://fsca.swissmedic.ch/mep/#?q=Vk_20151105_03
  • Notes / Alertes
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 Switzerland.
  • Notes supplémentaires dans les données

Device

Optisure Dual Coil Defibrillation lead
  • Modèle / numéro de série
    LDA 220 Q52, LDA 220 Q58, LDA 220 Q65 and LDP 220 Q58 | Total of 1121 leads are affected. Of which 164 have been implanted or are in hospital inventory outside US.
  • Classification du dispositif
    Cardiovascular Devices
  • Description du dispositif
    AIMD: Endocardial defibrillation lead
  • Manufacturer
    St. Jude Medical

Manufacturer

St. Jude Medical
  • Société-mère du fabricant (2017)
    Abbott Laboratories
  • Commentaire du fabricant
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    SATP