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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Terumo cardiovascular systems (terumo cvs) has become aware that under certain circumstances a terumo advanced perfusion system 1 centrifugal pump "service pump" message may display due to user induced motor movement. in this instance the terumo system 1 will recognize the movement (as it is designed to do} and display a "service pump" message. the user might interpret this message as a pump that requires service rather than a message displayed due to pump movement while not activated. because of these instructions the user may unnecessarily remove and replace a properly functioning piece of equipment (if the message was due to a user-induced action).