Events

Recall of 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
    19955
  • Event Initiated Date
    2016-04-01
  • Event Country
    New Zealand
  • Event Source
    NZMMDSA
  • Event Source URL
    https://medsafe.govt.nz/hot/Recalls/RecallSearch.asp
  • 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
    The power plug, which has been delivered with the system is not according to the local regulation in new zealand (as/nzs 3115:2000)., the pins of the plug can be touched when the plug is not inserted completely into the mains outlet, potentially exposing the person to electrical shock.
  • Action
    Product to be exchanged

Device

Mobile Digital X Ray System

Manufacturer

Philips Medical Systems DMC GmbH
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    NZMMDSA