Events

Recall of DIAGNOST 94

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PHILIPS ELECTRONICS LTD..

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
    65449
  • Event Risk Class
    II
  • Event Initiated Date
    2008-08-01
  • Event Country
    Canada
  • 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 bed exposures in a 90 degree tilted table position and a tube arm swing of 90 degrees the tube arm may be moved down to a critical position where it can collide with the patient bed or others.

Device

DIAGNOST 94
  • Model / Serial
    Model Catalog: (Lot serial: ); Model Catalog: MRC 0651 (Lot serial: ); Model Catalog: MII 3061 (Lot serial: )
  • Product Description
    DIAGNOST 94
  • Manufacturer
    PHILIPS ELECTRONICS LTD.

Manufacturer

PHILIPS ELECTRONICS LTD.
  • Manufacturer Address
    MARKHAM
  • Manufacturer Parent Company (2017)
    Philips
  • Source
    HC