Events

Recall of SOFTBANK II 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
    55480
  • Event Risk Class
    II
  • Event Initiated Date
    2010-07-26
  • 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
    Functionality issue: when softbank history reports for multiple patients were generated using softreports. if more than one qualifying patient each qualified patient has a report but all orders are listed under each patient even those that do not belong to them. there is no way to distinguish what results belong to a specific patient.

Device

SOFTBANK II SOFTWARE
  • Model / Serial
    Model Catalog: (Lot serial: 23.2.0.x); Model Catalog: (Lot serial: 23.1.2.x); Model Catalog: (Lot serial: 25.0.0.x)
  • Product Description
    SoftBank II v.23.1.2.x 23.2.0.x25.0.0
  • Manufacturer
    SCC SOFT COMPUTER

Manufacturer

SCC SOFT COMPUTER