Recall of OMRON 3 WAY INSTANT THERMOMETER MC 600

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by OMRON HEALTHCARE 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
    56517
  • Event Risk Class
    II
  • Event Initiated Date
    2005-10-24
  • 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
    Omron healthcare inc. has received consumer complaints that the tip of the thermometer overheated during use. consumers complained of discomfort during use and several reported redness/blistering of the skin.

Device

  • Model / Serial
    Model Catalog: MC-600CAN (Lot serial: 01-38); Model Catalog: MC-600CAN (Lot serial: 01-37); Model Catalog: MC-600CAN (Lot serial: 01-36); Model Catalog: MC-600CAN (Lot serial: MC-600CAN); Model Catalog: MC-600CAN (Lot serial: 01-32)
  • Product Description
    OMRON 3-WAY INSTANT THERMOMETER
  • Manufacturer

Manufacturer

  • Manufacturer Address
    LAKE FOREST
  • Source
    HC