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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Decrochement de la traverse. la cause initiale de cette defaillance est la contamination de la matiere premiere de l'arbre pivot qui retient la traverse.
Model Catalog: KM560108 (Lot serial: ENTRE KM56-10015 ET KM56-11074); Model Catalog: KM560104 (Lot serial: ENTRE KM56-10015 ET KM56-11074); Model Catalog: KM560101 (Lot serial: ENTRE KM56-10015 ET KM56-11074); Model Catalog: KM560184 (Lot serial: ENTRE KM56-10015 ET KM56-11074); Model Catalog: KM560188 (Lot serial: ENTRE KM56-10015 ET KM56-11074); Model Catalog: KM560181 (Lot serial: ENTRE KM56-10015 ET KM56-11074)