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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It has been identified that the spider 2 limb positioner may unlock (loss of traction) resulting in the potential movement of the patient when the device is within close proximity to an rf (radiofrequency) source. loss of traction can potentially result in the unintended repositioning of the extremity within traction. there is a potential for tissue or cartilage damage to occur due to the unexpected and sudden repositioning.