Recall of VITROS 5600 INTEGRATED SYSTEM - SOFTWARE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by ORTHO-CLINICAL DIAGNOSTICS.

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
    83283
  • Event Risk Class
    II
  • Event Initiated Date
    2009-05-29
  • 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
    Complaint received of biased glucose result on a vitros 5600 integrated system. investigation has found that under a very specific set of circumstances when the display/report is configured by the operator an erroneous result could be generated by the vitros 5600 integrated system.

Device

  • Model / Serial
    Model Catalog: 680 2863 (Lot serial: 56000337); Model Catalog: 680 2863 (Lot serial: 56000336); Model Catalog: 680 2863 (Lot serial: 56000136); Model Catalog: 680 2865 (Lot serial: 36000116); Model Catalog: 680 2863 (Lot serial: 56000298); Model Catalog: 680 2863 (Lot serial: 56000193); Model Catalog: 680 2865 (Lot serial: 36000130); Model Catalog: 680 2863 (Lot serial: 56000124)
  • Product Description
    VITROS 5600 INTEGRATED SYSTEM SOFTWARE
  • Manufacturer

Manufacturer