Events

Recall of ARTIS ZEEGO MULTI-AXIS

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

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
    92332
  • Event Risk Class
    III
  • Event Initiated Date
    2013-03-05
  • 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
    A potential issue on artis systems with the software artis vc20x/vc21a/vd10x that have a dsa licence installed has been identified. under certain preconditions executing roadmap ogp (organ program) in the dsa overlay mode may lead to imprecise registration of the dsa mask image with the roadmap image displayed on the live monitor.

Device

ARTIS ZEEGO MULTI-AXIS
  • Model / Serial
    Model Catalog: 10280959 (Lot serial: N/A FOR ALL); Model Catalog: 10094141 (Lot serial: ); Model Catalog: 10094135 (Lot serial: ); Model Catalog: 10094137 (Lot serial: ); Model Catalog: 10094139 (Lot serial: )
  • Product Description
    ARTIS ZEEGO MULTI-AXIS
  • Manufacturer
    SIEMENS HEALTHCARE LIMITED

Manufacturer

SIEMENS HEALTHCARE LIMITED
  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
    Siemens Ag
  • Source
    HC