Field Safety Notices about Scooter Sungift 500

According to Health Products Regulatory Authority, this field safety notices involved a device in Ireland that was produced by Sungift PLC.

What is this?

Field safety notices are communications sent out by medical device manufacturers or their representatives in relation to actions that they may be taking in relation to their product that is on the market. These are mainly for health workers, but also for users. They can include recalls and alerts.

Learn more about the data here
  • Type of Event
    Field Safety Notice
  • Event Number
    SN2006(04)
  • Date
    2006-06-21
  • Event Country
  • Event Source
    HPRA
  • Event Source URL
  • Notes / Alerts
    "Irish data is current through April 2019. All of the data comes from the Health Products Regulatory Authority (Ireland), 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 data from the U.S. and Ireland."
  • Extra notes in the data
  • Reason
    Recall of the sungift 500 battery powered scooters.
  • Action
    Examine the scooters you have in your stock to determine if you have any Sungift 500 scooters.  If you find one of these devices stop using it immediately, take it out of service and advise the Irish Medicines Board.

Device

  • Model / Serial
  • Product Description
    Scooter Sungift 500
  • Manufacturer

Manufacturer

  • Source
    HPRA