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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During factory internal testing of this device philips identified wear of the main steel cable which supports the u-shaped swivel arm. consequently the cable might break prematurely outside of the specifications set for the cable (lifetime 50000 cycles). if the cable breaks the built in safety catch may not adequately prevent the unit from falling down.