Events

Recall of CT 9000 CONTRAST DELIVERY SYSTEM - INJECTOR

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PHILIPS MEDICAL SYSTEMS CANADA A DIVISION OF 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
    21149
  • Event Risk Class
    I
  • Event Initiated Date
    1995-02-21
  • 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

Device

CT 9000 CONTRAST DELIVERY SYSTEM - INJECTOR
  • Model / Serial
    Model Catalog: 800099 (Lot serial: 3574); Model Catalog: 601195 (Lot serial: 3574); Model Catalog: 800099 (Lot serial: 3564); Model Catalog: 601195 (Lot serial: 3624); Model Catalog: 800099 (Lot serial: ANY LOT # HIGHER THAN 405750); Model Catalog: 601195 (Lot serial: ANY LOT # HIGHER THAN 405750); Model Catalog: 800099 (Lot serial: 3624); Model Catalog: 601195 (Lot serial: 3564)
  • Manufacturer
    PHILIPS MEDICAL SYSTEMS CANADA A DIVISION OF PHILIPS ELECTRONICS LTD.

Manufacturer

PHILIPS MEDICAL SYSTEMS CANADA A DIVISION OF PHILIPS ELECTRONICS LTD.
  • Manufacturer Address
    BRAMPTON
  • Source
    HC