Field Safety Notices about NIPPY 3 ventilator, NIPPY JUNIOR ventilator, NIPPY ST ventilator, NIPPY S ventilator

According to Health Products Regulatory Authority, this field safety notices involved a device in Ireland that was produced by B&D Electromedical.

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
    SN2013(13)
  • Date
    2013-11-08
  • 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
    The use of oxygen with these devices is not recommended.
  • Action
    1. Ensure that all device users are aware of the information provided in the  attached field safety notice (FSN) issued recently by B&D Electromedical.  2. Ensure that medical staff are aware of the potential risks of using equipment  not designed for use with oxygen.  3. Users who have concerns with the device are encouraged to remove the  device from use and contact the distributor Respicare Ltd Medical Centre.

Device

  • Model / Serial
  • Product Description
    NIPPY 3 ventilator, NIPPY JUNIOR ventilator, NIPPY ST ventilator, NIPPY S ventilator
  • Manufacturer

Manufacturer