Events

Recall of COULTER LH SLIDESTAINER/SLIDEMAKER

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
    62989
  • Event Risk Class
    II
  • Event Initiated Date
    2008-06-12
  • 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 sample id information embedded in the barcode (machine readable black and white bars) that is printed and affixed on a slide made by the slidemaker does not match the human readable portion (text).

Device

COULTER LH SLIDESTAINER/SLIDEMAKER
  • Model / Serial
    Model Catalog: 6605633 (Lot serial: Registration number 32489)
  • Product Description
    COULTER LH SlideMaker
  • Manufacturer
    BECKMAN COULTER CANADA L.P.

Manufacturer

BECKMAN COULTER CANADA L.P.