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 that the two bolts that attach the clamping plate to the lateral shaft may break. this may cause the c-arm to float freely. depending on the orientation of the free-floating c-arm and any other forces applied to it the c-arm could move laterally forward slide out of its bearings and then possibly sag.