Recall of Philips MobileDiagnost wDR Mobile Digital X Ray System

According to New Zealand Medicines and Medical Devices Safety Authority, this recall involved a device in New Zealand that was produced by Philips Medical Systems DMC GmbH.

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
    16733
  • Event Initiated Date
    2014-05-19
  • 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: Philips New Zealand Commercial Limited, Level 3, 123 Carlton Gore Road, Newmarket, AUCKLAND 1023
  • Reason
    Under very specific error conditions the system executes an unintended exposure:, * the hand switch is erroneously stuck in pressed position, while the system is switched off,, * the system is powered up with the hand switch in that erroneous condition,, * the user logs in, selects a patient for examination, gets a green ready light in,, * the examination context, if the tube arm is then moved out of the zero position, the system is doing an exposure.
  • Action
    Software to be upgraded

Manufacturer

  • Manufacturer Parent Company (2017)
  • Source
    NZMMDSA