Events

Field Safety Notices about Cordis PRECISE® PRO RX

According to Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), this field safety notices involved a device in Slovenia that was produced by Cordis.

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
  • Date
    2016-05-04
  • Event Country
    Slovenia
  • Event Source
    AMPMDRS
  • Notes / Alerts
    Data from Slovenia is current through February 2019. All of the data comes from the Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (via FOI), 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 Slovenia.
  • Extra notes in the data
  • Reason
    Based on recent complaints and a related investigation, cordis found that the products made between april 27, 2015 and november 22, 2015 (series in table 1) were associated with an increase in incidents that caused installation and installation problems. in certain cases the separation of the outer member of the sleeve, resulting in the stent being prevented or only partially installed. .

Device

Cordis PRECISE® PRO RX
  • Model / Serial
  • Manufacturer
    Cordis

Manufacturer

Cordis