Events

Recall of BACT/VIEW SOFTWARE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BIOMERIEUX CANADA INC..

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
    121381
  • Event Risk Class
    II
  • Event Initiated Date
    2006-01-12
  • 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
    Une corruption de la base de donnees du bact/view pourrait entrainer l'echec de transmission des resultats positifs au systeme d'information du laboratoire et retarder la prise en charge du patient.

Device

BACT/VIEW SOFTWARE
  • Model / Serial
    Model Catalog: (Lot serial: )
  • Product Description
    BACT/VIEW SYSTEM
  • Manufacturer
    BIOMERIEUX CANADA INC.

Manufacturer

BIOMERIEUX CANADA INC.