Events

Recall of TOTALCARE BED SYSTEM TREATMENT SURFACE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by HILL-ROM CANADA LTD..

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
    87772
  • Event Risk Class
    II
  • Event Initiated Date
    2009-12-28
  • 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
    Beds may experience problems with a cable that control nurse call bed movement and entertainment functions from the intermediate side rail.Some of the individual conductors within cable may fail prematurely.

Device

TOTALCARE BED SYSTEM TREATMENT SURFACE
  • Model / Serial
    Model Catalog: P1900 (Lot serial: K285AM5539 TO K310AM5864)
  • Product Description
    totalcare bed system
  • Manufacturer
    HILL-ROM CANADA LTD.

Manufacturer

HILL-ROM CANADA LTD.