Events

Recall of Intelerad Picture Archiving and Communication System

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

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
    22338
  • Event Initiated Date
    2017-12-12
  • 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: Pharmaceutical Marketing New Zealand Ltd, 162 Nile Road, Milford, Auckland 0620
  • Reason
    When viewing a report, the less than character (<) is not present, while it was there in the original report received by intelepacs. in other cases, when the character is present in a combination with other characters , parts of the report text following the less than character are not displayed, depending on the intelerad application used by the end-user to review the reports.
  • Action
    Software to be upgraded

Device

Intelerad Picture Archiving and Communication System

Manufacturer

Intelerad Medical Systems Incorporated