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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Incorrectly installed f1 fuse on the avea ventilator tca board may result in a failed/blown fuse causing loss of power to the uim and inop condition during pre-use check or during use with cessation of ventilation to the patient. audible clinical alarm is activated.