Recall of UNO 102 PATIENT LIFT

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by PERIDOT MEDICAL 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
    13993
  • Event Risk Class
    II
  • Event Initiated Date
    2008-11-05
  • 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
    Certain liko uno patient lifts are being recalled because the actuator of the lift has the potential to separate when the upper arm is fully extended which may result in a patient fall.

Device

  • Model / Serial
    Model Catalog: UNO 102 EM (Lot serial: 20001-21300); Model Catalog: UNO 102 (Lot serial: 20001-21300); Model Catalog: UNO 102 (Lot serial: 30001-48100); Model Catalog: UNO 102 EM (Lot serial: 30001-48100); Model Catalog: UNO 102 ES (Lot serial: 30001-48100); Model Catalog: UNO 102 EE (Lot serial: 30001-48100); Model Catalog: UNO 102 ES (Lot serial: 20001-21300); Model Catalog: UNO 102 EE (Lot serial: 20001-21300); Model Catalog: UNO 100 EE (Lot serial: 7090001-7096200); Model Catalog: UNO 100 EM (Lot serial: 7090001-7096200); Model Catalog: UNO 101 (Lot serial: 10001-11000)
  • Product Description
    LIKO UNO 102 PATIENT LIFT
  • Manufacturer

Manufacturer