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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If scheduled orders are documented and edited prior to the orders' original schedule time carevue chart release c.0 (running on the dc7100 computers of the intellivue mp700 patient monitor system) can create a second instance of the same order marked as pending if the following conditions occur: 1. an order or intervention is entered as a scheduled administration and 2. a clinician charts the pending order earlier than scheduled and 3. a user/clinician changes edits or acknowledges the order.