Events

Recall of MIM (SOFTWARE PACKAGE)

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

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
    15669
  • Event Risk Class
    III
  • Event Initiated Date
    2008-05-27
  • 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
    Reported that the suv tool reports different values (max suv) for a small tumor depending on whether the pet is opened alone or whether the pet is participating in a fusion with a ct.

Device

MIM (SOFTWARE PACKAGE)
  • Model / Serial
    Model Catalog: (Lot serial: ALL LOT NUMBERS)
  • Product Description
    MIM SOFTWARE 4.0.2-4.0.5 4.1.0-4.1.2
  • Manufacturer
    MIM SOFTWARE INC.

Manufacturer

MIM SOFTWARE INC.
  • Manufacturer Address
    CLEVELAND
  • Manufacturer Parent Company (2017)
    Mim Software Inc.
  • Source
    HC