Events

Recall of UNICEL DXC 800

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
    51117
  • Event Risk Class
    III
  • Event Initiated Date
    2012-09-05
  • 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
    Beckman coulter has confirmed that the shuttle to barcode reader and cap piercer alignment procedure cannot be performed on dxc pro systems when the cap piercer is disabled. there is no impact if the cap piercer is not disabled and operating properly.

Device

UNICEL DXC 800
  • Model / Serial
    Model Catalog: 4764 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 4767 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 4764 (Lot serial: 139); Model Catalog: 4764 (Lot serial: 356); Model Catalog: 4764 (Lot serial: 1512)
  • Product Description
    UNICEL DXC 800 PRO
  • Manufacturer
    BECKMAN COULTER CANADA L.P.

Manufacturer

BECKMAN COULTER CANADA L.P.