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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Icu medical inc. has identified certain stopcocks that are incorporated in i.V sets may contain a metallic burr. out of an abundance of caution icu medical inc. is voluntarily recalling the affected devices. the company has not received complaints or reports of any patient injury associated with this issue.