Events

Recall of SYNCHRON LXI 725

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by BECKMAN COULTER 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
    27862
  • Event Risk Class
    II
  • Event Initiated Date
    2003-09-30
  • 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

SYNCHRON LXI 725
  • Model / Serial
    Model Catalog: (Lot serial: 475225 475225); Model Catalog: (Lot serial: SYNCHRON LX 20PRO P/N 476100); Model Catalog: (Lot serial: SYNCHRON LXi P/N 388983); Model Catalog: (Lot serial: SYNCHRON LX P/N 466100 466200)
  • Product Description
    SYNCHRON LX SOFTWARE 2TO2.33.4&4.1
  • Manufacturer
    BECKMAN COULTER INC.

Manufacturer

BECKMAN COULTER INC.