Recall of YSIO RADIOGRAPHY X-RAY SYSTEM - FULL MOTORIZED

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
    35588
  • Event Risk Class
    III
  • Event Initiated Date
    2013-08-28
  • Event Country
  • 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
    During a rad examination with automatic exposure control a highly unlikely malfunction can result in radiation continuing longer than required. this may also result in an overexposed image that is not of diagnostic quality so that the examination needs to be repeated. statistically this malfunction only occurs once every 7000 images and only if images are taken in automatic exposure mode.

Device

  • Model / Serial
    Model Catalog: 10281013 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 10094200 (Lot serial: 3025); Model Catalog: 10094200 (Lot serial: 3184); Model Catalog: 10094200 (Lot serial: 3208); Model Catalog: 10094200 (Lot serial: 3190)
  • Product Description
    YSIO
  • Manufacturer

Manufacturer

  • Manufacturer Address
    OAKVILLE
  • Manufacturer Parent Company (2017)
  • Source
    HC