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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Manufacturer has issued a communication to all customers with information on recommended blood tubing sets to be used with baxter instruments and positioning of these blood tubing sets.
Model Catalog: ARENASPX-BH (Lot serial: ALL SERIAL NUMBERS); Model Catalog: ARENASPX-BDH (Lot serial: ALL SERIAL NUMBERS); Model Catalog: ARENASPX-H (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3DPHA (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3DPA (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3PHA (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3PH (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3P (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3PHDP (Lot serial: ALL SERIAL NUMBERS); Model Catalog: STS1000-L3PDP (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SYS1000-L3PA (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 5M5551 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: ARENASPP-DH (Lot serial: ALL SERIAL NUMBERS); Model Catalog: ARENASPP-D (Lot serial: ALL SERIAL NUMBERS); Model Catalog: ARENA SPP (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 5M5538 (Lot serial: ALL SERIAL NUMBERS)