Events

Field Safety Notices about Liko SlingBar 350, SlingBar 360, SlingBar Wide 670, SideBar Standard. Part Numbers: 3156015, 3156002, 3156008,3156004, 3156013, 3156012, 3156017 or 3156011. Distributed between April 1998 and May 2008.

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

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
    SN2014(38)
  • Date
    2014-09-26
  • Event Country
    Ireland
  • Event Source
    HPRA
  • Event Source URL
    http://www.hpra.ie/homepage/medical-devices/safety-information/safety-notices/item?t=/SN201438&id=a94c0126-9782-6eee-9b55-ff00008c97d0
  • 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

Device

Liko SlingBar 350, SlingBar 360, SlingBar Wide 670, SideBar Standard. Part Numbers: 3156015, 3156...
  • Model / Serial
  • Product Description
    Liko SlingBar 350, SlingBar 360, SlingBar Wide 670, SideBar Standard. Part Numbers: 3156015, 3156002, 3156008,3156004, 3156013, 3156012, 3156017 or 3156011. Distributed between April 1998 and May 2008. Priority 2 – Warning
  • Manufacturer
    Liko

Manufacturer

Liko