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.
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Philips healthcare has discovered a problem in the philips ultrasound q-station software version 3.0 or higher that could result in measurements from a study to be appended to subsequent studies for other patients. if a healthcare provider makes a clinical decision on the sole basis of these measurements without considering other available clinical data misdiagnosis and/or delayed or incorrect therapy may result.