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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A lamp available for use as an optional accessory with the terumo advanced perfusion system 1 sarns modular perfusion system 8000 and sarns perfusion system 9000 uses a halogen bulb which will become hot during use. this correction is to notify users that the lamp will become hot and can cause damage or ignition to materials that are placed in close proximity to the lamp housing.