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 is possible that the distal part of the anchor may break on insertion into bone during surgery. the surgery may be completed using an alternate fixation device and in most cases the broken anchor piece can be retrieved with a grasper or sharp instrument. if however the surgeon is unable to locate the broken piece the patient may be subject to x-ray. an additional incision may be required to remove the broken piece.