Recall of UNICEL DXH 800 COULTER CELLULAR ANALYSIS SYSTEM

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
    64659
  • Event Risk Class
    II
  • Event Initiated Date
    2017-11-07
  • Event Country
  • 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 shield for the single-tube station on the dxh instrument may interfere with sample aspiration in the open vial position. the mechanical interference between the shield and the right (green) position of the single-tube station can cause the tube holder to remain in the down position during aspiration and then spring up resulting in the dislodging of an open vial. this mechanical interference may result in a biohazardous spill. the left (lavender) position tube holder of the manual station is not impacted by this issue.

Device

  • Model / Serial
    Model Catalog: B24802 (Lot serial: SW VERSION 3.1.1.0); Model Catalog: 629029 (Lot serial: SERIAL # AS23151); Model Catalog: B24802 (Lot serial: SERIAL # AS23151); Model Catalog: 629029 (Lot serial: SW VERSION 3.1.1.0)
  • Product Description
    UNICEL DXH 800 CELLULAR ANALYSIS SYSTEM
  • Manufacturer

Manufacturer