Events

Recall of LIKO MULTIRALL CEILING LIFT

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
    36862
  • Event Risk Class
    II
  • Event Initiated Date
    2017-08-24
  • 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
    Hill-rom has become aware of a user error of improperly attaching the multiralltm 200 overhead lift to the s65 carriage that could result in a potential safety issue.

Device

LIKO MULTIRALL CEILING LIFT
  • Model / Serial
    Model Catalog: 3136011 (Lot serial: NA)
  • Product Description
    LIKO MULTIRALL CEILING LIFT S65 Carriage
  • Manufacturer
    HILL-ROM CANADA LTD.

Manufacturer

HILL-ROM CANADA LTD.