Events

Recall of ALLOGREFFE VALVULAIRE AORTIQUE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by HEMA-QUEBEC.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    131429
  • Event Risk Class
    III
  • Event Initiated Date
    2012-09-20
  • Event Country
    Canada
  • Event Source
    HC
  • Notes / Alerts
    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.
  • Extra notes in the data
  • Reason
    Risque potentiel de defectuosite de la pochette externe de l'emballage. les scelles de la pochette pourraient contenir des imperfections sur l'un ou l'autre des cotes adjacents au chevron en " v ". cela pourrait entrainer la perte de la sterilite de l'exterieur de la pochette interne.

Device

ALLOGREFFE VALVULAIRE AORTIQUE
  • Model / Serial
    Model Catalog: AORTIQUE (Lot serial: ); Model Catalog: PULMONAIRE (Lot serial: )
  • Product Description
    Allogreffe valvulaire Aortique
  • Manufacturer
    HEMA-QUEBEC

Manufacturer

HEMA-QUEBEC
  • Manufacturer Address
    QUEBEC
  • Manufacturer Parent Company (2017)
    Héma-Québec
  • Source
    HC