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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Baxter is sending an important safety update to the instructions for use for baxter peritoneal dialysis (pd) transfer sets titanium adapters disconnect caps and connection shield product codes. specifically baxter is adding contraindication statements to address iodine allergy for baxter's pd products which contain iodine (i.E. povidone iodine) or for which iodine use is recommended. there is no product hold or physical removal of devices from the field associated with this action.