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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Reports of component performance errors during product use and baxter intends to bring these products in line with baxter high standards of quality.
Model Catalog: SYS1000-L3P (Lot serial: S/N 01001-S/N 15894); Model Catalog: K100CIT (Lot serial: ALL PRODUCTS LABELLED SYSTEM); Model Catalog: N1000DP (Lot serial: S/N 01001-S/N 15894); Model Catalog: K100S05 (Lot serial: S/N 01001-S/N 15894); Model Catalog: K100CIT (Lot serial: S/N 01001-S/N 15894); Model Catalog: SYS1000-L3P (Lot serial: 1000 AND TINA); Model Catalog: N100HCT (Lot serial: 1000 AND TINA); Model Catalog: N1000DP (Lot serial: 1000 AND TINA); Model Catalog: K100S05 (Lot serial: 1000 AND TINA); Model Catalog: K100CIT (Lot serial: 1000 AND TINA); Model Catalog: SYS1000-L3P (Lot serial: ALL PRODUCTS LABELLED SYSTEM); Model Catalog: N100HCT (Lot serial: ALL PRODUCTS LABELLED SYSTEM); Model Catalog: N1000DP (Lot serial: ALL PRODUCTS LABELLED SYSTEM); Model Catalog: K100S05 (Lot serial: ALL PRODUCTS LABELLED SYSTEM); Model Catalog: N100HCT (Lot serial: S/N 01001-S/N 15894)