Events

Recall of MYLAB30CV ULTRASOUND SYSTEM

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BRACCO DIAGNOSTICS 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
    35006
  • Event Risk Class
    II
  • Event Initiated Date
    2005-10-11
  • 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
    Archived patient data files may under certain conditions be corrupted upon reopening of the file.

Device

MYLAB30CV ULTRASOUND SYSTEM
  • Model / Serial
    Model Catalog: 9807300001 (Lot serial: )
  • Product Description
    MYLAB 30CV ULTRASOUND SYSTEM
  • Manufacturer
    BRACCO DIAGNOSTICS CANADA INC.

Manufacturer

BRACCO DIAGNOSTICS CANADA INC.
  • Manufacturer Address
    VAUGHAN
  • Manufacturer Parent Company (2017)
    Bracco Spa
  • Source
    HC