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 has become aware of the following issues: 1. if the pins that connect the battery to the device have become damaged or full of debris the device may not power on or may repetitively reboot. 2. when the device is unplugged from ac mains it may enter a state where it will not charge for shock delivery or may unexpectedly cease pacing.