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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Corflex was informed from a component supplier that they have identified an out of spec part that was shipped to corflex and may have been used in the manufacturing of the contender post-op knee brace. product defect was not obvious to the eye it was in the drop lock feature which is not commonly used by c. turner medical's facilities.
Model Catalog: 75-7500-231 (Lot serial: all units); Model Catalog: 75-7500-011 (Lot serial: all units); Model Catalog: 75-7500-038 (Lot serial: all units); Model Catalog: 75-7550-000 (Lot serial: all units); Model Catalog: 75-7500-000 (Lot serial: all units); Model Catalog: 75-7500-087 (Lot serial: all units); Model Catalog: 75-7500-075 (Lot serial: all units)