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 smiths medical portex abl syringes component 4042-2 found in the kits are being recalled by smiths medical. this action has been initiated due to an issue when abl syringes are used with radiometer blood gas analyzers.