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 received reports from the field stating the patient table on a system had an unexpected downward movement while a patient was on the table. philips has determined that the cause was a malfunction of the vertical brake of the patient support due to embrittlement of the vertical brake's screws.