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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Carefusion is aware of three significant events involving alaris syringe pumps administering into a high negative (vacuum) pressure patient line which resulted in a bolus. this condition may exist where the infusion line is shared with other high pressure medical cardiopulmonary bypass pumps or haemodialysis pumps.
Model Catalog: 80053UN01 (Lot serial: MORE THAN SERIAL NUMBERS); Model Catalog: 80033UND1 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 80043UN01 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 80023UN01 (Lot serial: MORE THAN 10 SERIAL NUMBERS)