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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It has been reported the elastic support strap on the product can slip through the buckle leading to abrupt loss of support from the device.
Model Catalog: RFU50002 (Lot serial: 651 and 706); Model Catalog: RFU500011 (Lot serial: 651 and 706); Model Catalog: RFU50001 (Lot serial: 651 and 706); Model Catalog: RFU500021 (Lot serial: all lot numbers from); Model Catalog: RFU50002 (Lot serial: all lot numbers from); Model Catalog: RFU50001 (Lot serial: all lot numbers from); Model Catalog: RFU500021 (Lot serial: 651 and 706); Model Catalog: RFU500011 (Lot serial: all lot numbers from)