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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The circlip may become hyperextended during installation or service or become deformed during use. this may create a ramping effect and may allow the arm to fall.
Model Catalog: 0682000850 (Lot serial: DEC 23 2003 AND SEP 30 2006); Model Catalog: 0682000851 (Lot serial: DEC 23 2003 AND SEP 30 2006); Model Catalog: 0682000852 (Lot serial: DEC 23 2003 AND SEP 30 2006); Model Catalog: 0682000850 (Lot serial: ALL LOTS DISTIRBUTED BETWEEN); Model Catalog: 0682000851 (Lot serial: ALL LOTS DISTIRBUTED BETWEEN); Model Catalog: 0682000852 (Lot serial: ALL LOTS DISTIRBUTED BETWEEN)