Recall of CERNER PROVISION WORKSTATION

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by CERNER CORPORATION.

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
    28383
  • Event Risk Class
    II
  • Event Initiated Date
    2011-09-15
  • 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
    This issue occurs because an older version of a non-clinical document can be displayed instead of the most recent version. typically the system displays the most recent version and the user can select to view older versions from the history window. however an older version of the document is displayed automatically when you do not select the older version or are aware that a newer version exists.

Device

  • Model / Serial
    Model Catalog: (Lot serial: Imaging 2007.18 35863); Model Catalog: (Lot serial: Imaging 2010.01 41919); Model Catalog: (Lot serial: Imaging 2010.02 45389); Model Catalog: (Lot serial: Imaging 2007.09 38896)
  • Product Description
    Cerner ProVision Document Imaging
  • Manufacturer

Manufacturer

  • Manufacturer Address
    KANSAS CITY
  • Manufacturer Parent Company (2017)
  • Source
    HC