Events

Recall of GIRAFFE SHUTTLE

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
    132527
  • Event Risk Class
    II
  • Event Initiated Date
    2015-07-15
  • 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
    Shortened battery life can lead to a loss of power to devices plugged into the shuttle. power loss during transport most reasonably expected to occur from this battery issue may lead to a minor delay in the transport time which may result in a minor decrease in body temperature (mild hypothermia). there have been no injuries reported as a result of this issue.

Device

GIRAFFE SHUTTLE
  • Model / Serial
    Model Catalog: M1143651 (Lot serial: > 10 numbers contact mfg)
  • Product Description
    Giraffe Shuttle
  • Manufacturer
    MAQUET-DYNAMED INC.

Manufacturer

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