Events

Recall of RADIANT WARMER

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by DRAEGER MEDICAL INFANT CARE 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
    17139
  • Event Risk Class
    II
  • Event Initiated Date
    1998-06-21
  • 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
    See description "field 14".

Device

RADIANT WARMER
  • Model / Serial
    Model Catalog: (Lot serial: SAME AS COMPANY ID 100305); Model Catalog: (Lot serial: MODELS RW82 AND RW81); Model Catalog: (Lot serial: MODEL WBR82); Model Catalog: (Lot serial: SAME AS COMPANY ID 107316)
  • Product Description
    RESUSCITAIRE RADIANT WARMER
  • Manufacturer
    DRAEGER MEDICAL INFANT CARE INC.

Manufacturer

DRAEGER MEDICAL INFANT CARE INC.
  • Manufacturer Address
    TELFORD
  • Source
    HC