Canadian data is current through March 2018. All of the data comes from Health Canada, 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 Canada.
데이터 추가 비고
원인
Philips has become aware that the philips heartstart mrx monitor/defibrillator when operating on battery power only may experience an unexpected shutdown if exposed to elevated levels of electromagnetic interference from rf energy sources. examples of equipment that can cause electromagnetic interference are medical devices cellular products information technology equipment and radio/television transmissions.