Events

Rappel de ABBOTT HI-TORQUE CONNECT STRAIGHT

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par ABBOTT VASCULAR A DIVISION OF ABBOTT LABORATORIES LTD..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    26234
  • Classe de risque de l'événement
    I
  • Date de mise en oeuvre de l'événement
    2013-11-22
  • Pays de l'événement
    Canada
  • Source de l'événement
    HC
  • Notes / Alertes
    Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
  • Notes supplémentaires dans les données
  • Cause
    A small number of ht connect peripheral guide wires have exhibited partial delamination of the ptfe coating. to date the frequency of worldwide reported incidents of delamination of the coating is 0.08%. while there have been no long term or irreversible patient effects reported potential risks associated with delamination of the coating include embolism thrombus and occlusion in peripheral vessels.

Device

ABBOTT HI-TORQUE CONNECT STRAIGHT
  • Modèle / numéro de série
    Model Catalog: 1012587 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012589 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012588 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012594 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012593 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012595 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012591 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012592 (Lot serial: > 10 numbers contact mfg); Model Catalog: 1012590 (Lot serial: > 10 numbers contact mfg)
  • Description du dispositif
    ABBOTT HI-TORQUE CONNECT STRAIGHT GUIDEWIRES
  • Manufacturer
    ABBOTT VASCULAR A DIVISION OF ABBOTT LABORATORIES LTD.

Manufacturer

ABBOTT VASCULAR A DIVISION OF ABBOTT LABORATORIES LTD.
  • Adresse du fabricant
    MISSISSAUGA
  • 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
    HC