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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Notice to customers with an additional warning to keep tubes and cables away from the patient's controls and that failure to do so may lead to accidental operation of the control keys and inadvertent movement of the mattress platform. if such movement could injure the patient use the function lockout to disable the controls when the paitent is unattended.