Events

Recall of LIAISON XL ANALYZER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DIASORIN 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
    144818
  • Event Risk Class
    III
  • Event Initiated Date
    2016-03-14
  • 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
    A software upgrade to the liaison xl analyzer activities will be conducted because the completed results in the "done" folder under the "results" tab may not be aligned properly until the software aut0-refreshes or after leaving and reentering the "done" folder.

Device

LIAISON XL ANALYZER
  • Model / Serial
    Model Catalog: I0050 (Lot serial: all lots); Model Catalog: I0050 (Lot serial: )
  • Product Description
    LIAISON XL ANALYZER;liaison xl analyzer
  • Manufacturer
    DIASORIN INC.

Manufacturer

DIASORIN INC.
  • Manufacturer Address
    STILLWATER
  • Manufacturer Parent Company (2017)
    DiaSorin SpA
  • Source
    HC