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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Components used in the production of trudell's nebulizer kits have been identified as recalled product manufactured by unomedical inc. the issue with the recalled oxygen masks is that there could be a sticky substance on the inside and/or outside of the mask that may manifest itself in approximately 6 to 8 months after manufacture of the product. the sticky masks could result in inconvenience and in some cases there is a remote possibility of potential harm to the patient.