Events

Recall of UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM - TOTAL T4 ASSAY

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BECKMAN COULTER CANADA L.P..

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
    87918
  • Event Risk Class
    II
  • Event Initiated Date
    2011-03-11
  • 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
    The concentration of total t4 in samples from pregnant women is erroneously low when measured using the access total t4 assay.

Device

UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM - TOTAL T4 ASSAY
  • Model / Serial
    Model Catalog: 33800 (Lot serial: ALL REAGENT PACKS)
  • Product Description
    UNICEL DXI 800 ACCESS IMMUNOASSAY SYSTEM - TOTAL T4 ASSAY
  • Manufacturer
    BECKMAN COULTER CANADA L.P.

Manufacturer

BECKMAN COULTER CANADA L.P.