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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The safety and performance of these devices has not been properly evaluated and so the ce marking of the devices is not valid. medicina therefore advises that the product is recalled from the market. the p700 and p900 pumps have previously been recalled however it is possible that not all of these devices have been returned and medicina requests that any devices with model numbers p500 p700 and p900 be returned to them.