Events

Field Safety Notices about DUAFIT 0°

According to Swiss Agency for Therapeutic Products, this field safety notices involved a device in Switzerland that was produced by In2Bones SAS.

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 ID
    Vk_20150317_27
  • Event Date Posted
    2015-03-23
  • Event Country
    Switzerland
  • Event Source
    SATP
  • Event Source URL
    https://fsca.swissmedic.ch/mep/#?q=Vk_20150317_27
  • Notes / Alerts
    The data from Switzerland is current through March 2018. All of the data comes from Swiss Agency for Therapeutic Products, 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 recall data from the U.S. and Switzerland.
  • Extra notes in the data

Device

DUAFIT 0°
  • Model / Serial
    A60 SP002, A60 SP003, A60 SP004 | 1404032 (expiry date 2019/05)1412011 (expiry date 2019/11)1412021 (expiry date 2019/11)1404034 (expiry date 2019/05)
  • Product Description
    MD: Ligament anchor
  • Manufacturer
    In2Bones SAS

Manufacturer

In2Bones SAS