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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Ge healthcare has recently become aware of the potential for the rotating iv pole to fall due to excessive tap drill depth resulting in a thin wall section of the block bracket assembly which is the bracket that attaches the pole to the bed. a fall could result in an injury to a bystander holding the patient or to the operator. there have been no injuries as a result of this issue.