Retiro De Equipo (Recall) de VTI Bayonet 20 MHz Doppler Probe (used for the intraoperative and transcutaneous critical evaluation of blood flow)

Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 Australia.