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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Users have complaints of catching their fingers under the seat bars.
Model Catalog: MDS809700 (Lot serial: 2005 AND JUNE 2007.); Model Catalog: MDS809650 (Lot serial: 2005 AND JUNE 2007.); Model Catalog: MDS809600 (Lot serial: 2005 AND JUNE 2007.); Model Catalog: MDS809850 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809800 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809750 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809700 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809650 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809600 (Lot serial: DEVICES PURCHASED BETWEEN JAN.); Model Catalog: MDS809750 (Lot serial: 2005 AND JUNE 2007.); Model Catalog: MDS809800 (Lot serial: 2005 AND JUNE 2007.); Model Catalog: MDS809850 (Lot serial: 2005 AND JUNE 2007.)