Events

Recall of SIMVIEW 3000 THERAPY SIMULATOR

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
    120540
  • Event Risk Class
    II
  • Event Initiated Date
    2008-12-11
  • 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
    The company has become aware of a potential for serious patient injury due to excessive wear that may occur to the drive belts used in the image intensifier and/or x-ray head drive mechanisms.

Device

SIMVIEW 3000 THERAPY SIMULATOR
  • Model / Serial
    Model Catalog: 1957153 (Lot serial: 4034); Model Catalog: 1957153 (Lot serial: 4011); Model Catalog: 5496992 (Lot serial: 6037); Model Catalog: 5496992 (Lot serial: 6038)
  • Product Description
    SIMVIEW 3000
  • Manufacturer
    SIEMENS CANADA LIMITED - HEALTHCARE

Manufacturer

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