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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Siemens healthcare has received a number of reports of gas cartridges failing to install on the rapidlab 348 and rapidlab 348ex instruments due to defective threads on the gas cartridges. the issue is intermittent and not all gas cartridges are affected.