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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A malfunction with one of the components that may result in the overheating of the pod has the potential to cause a burn if the pod is in direct contact with the patient.
Model Catalog: (Lot serial: 500549361); Model Catalog: (Lot serial: 500849360); Model Catalog: (Lot serial: 500849358); Model Catalog: (Lot serial: SN 500849356); Model Catalog: (Lot serial: 500874926); Model Catalog: (Lot serial: 500857064); Model Catalog: (Lot serial: 500823174)