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 received multiple reports since 2004 of malfunctions related to components of the sarns centrifugal system including the centrifugal system for the sarns perfusion system 9000. the reports can be broadly categorized as follows: loss of forward flow motor noise/vibration missing/inaccurate flow data erratic operation unexpected error messages/alarms module reset and smoke was seen or smelled.