Avis De Sécurité sur limitations in the use of the vidas lyme igg test, catalog no. 30320, and vidas 3 analyzer with the software version v1.1.4, catalog number 412590

Polish data is current through November 2018. All of the data comes from the Office for Registration of Medicinal Products, Medical Devices and Biocidal 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 Poland.