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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Stryker has become aware that there is a likelihood that the teletom series 4 & 6 controls and brakes will not work properly due to fluid intrusion within the control switches. if the teletom series 4 & 6 exhibit unintended movement or the controls and brakes fail it could potentially cause serious injuries to healthcare providers.