Events

Recall of YUNO TABLE EXTENSION DEVICE

According to Health Canada (via FOI), this recall involved a device in Canada that was produced by MAQUET-DYNAMED 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
    23568
  • Event Risk Class
    III
  • Event Initiated Date
    2013-04-15
  • 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
    By fully actuating the lever of the extension device handle skin can enter a gap between the handle lever and a recess in the handle bar. when the lever is released skin which might be within the gap could be pinched or cut.

Device

YUNO TABLE EXTENSION DEVICE
  • Model / Serial
    Model Catalog: 1433.62A0 (Lot serial: Part 1433.62A0 All SNs); Model Catalog: 1433.62A1 (Lot serial: Part 1433.62A1 SN 1 to 90); Model Catalog: 1433.62A0 (Lot serial: Part 1433.62A1 SN 1 to 90); Model Catalog: 1433.62A1 (Lot serial: Part 1433.62A0 All SNs)
  • Product Description
    YUNO Table Extension Device
  • Manufacturer
    MAQUET-DYNAMED INC.

Manufacturer

MAQUET-DYNAMED INC.
  • Manufacturer Address
    MISSISSAUGA
  • Manufacturer Parent Company (2017)
    Getinge AB
  • Source
    HC