Alerta De Seguridad para Probe Urethral Deskart Injet, registry nº 80074020004, Probe for Tracheal Aspiration Deskat Injet, registry nº 80074020005

Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.

To determine, as a measure of sanitary interest, the suspension of the manufacture, dissemination, distribution, trade and use, throughout the national territory, of all lots of products Uretral Deskart Injet, registration no. 80074020004, registration no. 80074020005, as they do not have a valid registration with Anvisa. The Technovigilance Unit / Anvisa will monitor the collection. #### UPDATED ON 08/18/2017, Field action filed by area. If necessary, the area can reassess the action at any time.