Events

Field Safety Notices about Implant Holder for SynFix-LR

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

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 Country
    Ireland
  • Event Source
    HPRA
  • Event Source URL
    http://www.hpra.ie/docs/default-source/Safety-Notices/fsnsummary_oct2010_qmsversion_final_061110-(2).pdf?sfvrsn=0
  • 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
    Advice has been provided by the manufacturer regarding the use of the device. 3rd Party Publications

Device

Implant Holder for SynFix-LR
  • Model / Serial
  • Product Description
    Implant Holder for SynFix-LR
  • Manufacturer
    Synthes GmbH

Manufacturer

Synthes GmbH