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 stopping distance being greater than what the user was familiar with from the prior version of the software a minor injury was reported as being related to one event and no additional reports of injury.
Model Catalog: (Lot serial: RTM-103497); Model Catalog: (Lot serial: RTM-103452); Model Catalog: (Lot serial: RTM-103423); Model Catalog: (Lot serial: RTM-103410); Model Catalog: (Lot serial: RTM-103407); Model Catalog: (Lot serial: RTM-103405); Model Catalog: (Lot serial: RTM-103752); Model Catalog: (Lot serial: RTM-103530)