Events

Recall of STEREOTACTIC COLLIMATOR

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

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
    41721
  • Event Risk Class
    II
  • Event Initiated Date
    2013-07-23
  • 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
    Device identification of the stereotactic circular collimator on an elekta digital linear accelerator with bar codes and a bar code scanner.

Device

STEREOTACTIC COLLIMATOR
  • Model / Serial
    Model Catalog: MRT 13521/X (Lot serial: ALL SERIAL NUMBERS)
  • Product Description
    STEREOTACTIC COLLIMATOR
  • Manufacturer
    ELEKTA INC.

Manufacturer

ELEKTA INC.
  • Manufacturer Address
    ATLANTA
  • Manufacturer Parent Company (2017)
    Elekta AB
  • Source
    HC