Events

Recall of SOFTPATH GUI SOFTWARE

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

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
    56657
  • Event Risk Class
    II
  • Event Initiated Date
    2011-08-10
  • 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
    For clients using a customized lab results ap macro or a micro results results ap macro in the patient report template there is a possibilility that the lab tests displayed may be only for the first order from the date range for the patient.

Device

SOFTPATH GUI SOFTWARE
  • Model / Serial
    Model Catalog: SOFTPATH GUI VERSIONS 4.2.3.3 TO 4.2.3.6 (Lot serial: ); Model Catalog: SOFTPATH GUI VERSIONS 4.3.0.5 TO 4.3.0.12 (Lot serial: )
  • Product Description
    SoftPath GUI versions 4.2.3.3 to 4.2.3.6 and 4.3.0.5 to 4.3.0.12
  • Manufacturer
    SCC SOFT COMPUTER

Manufacturer

SCC SOFT COMPUTER