Field Safety Notices about COLUMBUS REV FEMUR SPACER DISTAL F5, F6, F7, 15 mm; COLUMBUS REV FEMUR SPACER POST, F5, F6, F7, 15 mm

According to Ministry of Health, State Institute for Drug Control, Coordination Center for Departmental Medical Information Systems, this field safety notices involved a device in Czechia that was produced by Aesculap AG.

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
    1335
  • Date
    2017-11-10
  • Event Country
  • Event Source
    MHSIDCCCDMIS
  • Event Source URL
  • Notes / Alerts
    Czech data is current through July 2018. All of the data comes from the Czech Public Registry of Medical Devices, 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 the Czech Republic.
  • Extra notes in the data

Device

  • Model / Serial
    Model Number: NR485K Batch Number: NR458K COLUMBUS REV FEMUR SPACER DISTAL F5 15MM 51468773, 51577362 NR486K COLUMBUS REV FEMUR SPACER DISTAL F6 15MM 51447588, 51503765, 51586632 NR487K COLUMBUS REV FEMUR SPACER DISTAL F7 15MM 51447589, 51468302 NR585K COLUMBUS REV FEMUR SPACER POST.F5 15MM 51447595, 51503760, 51589205 NR586K COLUMBUS REV FEMUR SPACER POST.F6 15MM 51447596, 51571394, 51586634 NR587K COLUMBUS REV FEMUR SPACER POST.F7 15MM 51447597, 51585136
  • Product Description
    Inactive implantable medical devices
  • Manufacturer

Manufacturer