Retiro De Equipo (Recall) de Herculite Ultra Herculite Ultra Unidose Refill C4 Enamel, Herculite Ultra Unidose Refill A2 Enamel, Herculite Ultra Unidose Refill A3.5 Enamel, Herculite Ultra Refill Syringe A2 Enamel

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.