Rappel de FiberOptix Ultra 8 IAB: 8Fr 30cc Ultra 8 IAB: 8Fr 30cc FiberOptix Ultra 8 IAB: 8Fr 40cc Ultra 8 IAB: 8Fr 40cc UltraFlex IAB: 7.5Fr 30cc UltraFlex IAB: 7.5Fr 35cc UltraFlex IAB: 7.5Fr 40cc RediGuard IAB: 7Fr 30cc Percutaneous Insertion Tray

Finnish data is current through April 2018. All of the data comes from Valvira - National Supervisory Authority for Welfare and Health, 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 Finland.

Source: FSCA