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 was determined that lot gy256 incorporates the nc version of the loxim transfer piece rather than the proper rc version. this error could result in the inability to drive the implant into the prepared osteotomy. the transfer piece would turn within the implant and the implant would not advance into the bone.