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.
데이터 추가 비고
원인
Nobel biocare has become aware through a customer complaint that select abutments of nobelprocera abutment zr for straumann bone lvi nc 3.3 have been machined incorrectly. the abutment consists of a zirconia portion and an adapter portion that fits into the implant. the adapter portion was machined larger than specifications. the abutment will therefore not fit into the implant.