Field Safety Notices about Defibtech DDU-100 series AED marketed under the brand names Lifeline AED, ReviveR AED and Lifeforce AED

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

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
    SN2012(18)
  • Date
    2012-12-17
  • 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
    Certain defibtech ddu-100 series aeds marketed under the brand names lifeline aed, reviver aed and lifeforce aed may not deliver therapy.
  • Action
    1. Ensure that the relevant personnel in your organisation are made aware of the attached FSN and its content.  2. Determine if you have purchased a device that is affected by this issue by reviewing the attached FSN.  3. If you have an affected device, please follow the instructions provided by Defibtech LLC in the attached FSN.

Device

  • Model / Serial
  • Product Classification
  • Product Description
    Defibtech DDU-100 series AED marketed under the brand names Lifeline AED, ReviveR AED and Lifeforce AED
  • Manufacturer

Manufacturer