Events

Recall of ACUSON ANTARES ULTRASOUND SYSTEM - MAIN UNIT WITH 5.0 UPGRADES

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by SIEMENS CANADA LIMITED - HEALTHCARE.

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
    132840
  • Event Risk Class
    II
  • Event Initiated Date
    2008-04-10
  • 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
    Measurements allowed on mpr's (multi planar reconstruction quadrants of 2d images) acquired with a 3d free hand sweep which are converted to clips. should not be allowed due to the inaccurate spatial geometry.

Device

ACUSON ANTARES ULTRASOUND SYSTEM - MAIN UNIT WITH 5.0 UPGRADES
  • Model / Serial
    Model Catalog: 10032746 (Lot serial: 115300); Model Catalog: 10032746 (Lot serial: 115416); Model Catalog: 10032746 (Lot serial: 113469)
  • Product Description
    ACUSON ANTARES
  • Manufacturer
    SIEMENS CANADA LIMITED - HEALTHCARE

Manufacturer

SIEMENS CANADA LIMITED - HEALTHCARE
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC