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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The markings on the guage are incorrect. the discrepancy may not be apparent to the user and could result in incorrect placement of the k-wire.
Model Catalog: 71117083 (Lot serial: ALL PRIOR TO 2009); Model Catalog: 71117083 (Lot serial: EXCLUDING 08KM20464 &); Model Catalog: 71117083 (Lot serial: EXCLUDING 08KM12521)