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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This recall activity is restricted to corrective action regarding the standard tip suction wand. due to an insufficient adhesive application the distal tip has the potential to come loose from the wand and fall into the patient's chest cavity during surgery. this would likely be identified during or prior to the procedure.