Recall of Siemens Artis zee and Artis zeego systems with triple focus x-ray tube assembly

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Siemens AG.

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
    18717
  • Event Initiated Date
    2015-06-22
  • Event Country
  • Event Source
    NZMMDSA
  • Event Source URL
  • Notes / Alerts
    Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
  • Extra notes in the data
    Recalling Organisation: Siemens Healthcare (NZ) Ltd, Millennium Centre, Part Level 2, Building A, 600 Great South Road, Ellerslie, AUCKLAND 1051
  • Reason
    The "small focus" of the 3 focal spot x-ray tube may sporadically fail and further radiation release will not be possible. a software patch was introduced for systems that had an x-ray tube assembly from a particular production lot in combination with specific software. now all potentially affected x-ray tube assemblies are to be replaced.
  • Action
    Product to be modified

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    NZMMDSA