Events

Rappel de PROCLAIM 5 ELITE IMPLANTABLE PULSE GENERATOR

Selon Health Canada (via FOI), ce/cet/cette rappel concerne un dispositif en/au/aux/à Canada qui a été fabriqué par ABBOTT MEDICAL CANADA INC..

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
    18709
  • Classe de risque de l'événement
    II
  • Date de mise en oeuvre de l'événement
    2017-09-12
  • 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
    Abbott is advising physicians that our company is aware of instances in which the elective replacement indicator (eri) in some devices has triggered earlier than intended. in these cases the eri alerts were triggered early due to an error in how the device calculates the actual remaining battery life in the impacted implantable pulse generators (ipg). abbott avise les medecins qu'elle a connaissance de cas ou l'indicateur de remplacement electif (ire) de certains dispositifs s'est active plus tot que prevu. dans ces cas l'ire s'est active de facon hative en raison d'une erreur dans la maniere dont le dispositif calcule la duree de vie restante reelle de la pile dans les generateurs d'impulsions electriques implantables (giei) concernes.

Device

PROCLAIM 5 ELITE IMPLANTABLE PULSE GENERATOR
  • Modèle / numéro de série
    Model Catalog: 3660 (Lot serial: N/A); Model Catalog: 3662 (Lot serial: N/A)
  • Description du dispositif
    PROCLAIM 5 ELITE IMPLANTABLE PULSE GENERATOR;PROCLAIM 7 ELITE IMPLANTABLE PULSE GENERATOR
  • Manufacturer
    ABBOTT MEDICAL CANADA INC.

Manufacturer

ABBOTT MEDICAL CANADA INC.
  • 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