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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Improper bending of malleable shaft to within one and a half inch of the device gray handle could cause failure of the hand piece. there is potential of injury to patient from a broken piece. dk.
Model Catalog: 134003 (Lot serial: Device id #134009); Model Catalog: 134009 (Lot serial: Device id #134006); Model Catalog: 134006 (Lot serial: Device id #134006); Model Catalog: 134003 (Lot serial: Device id #134006); Model Catalog: 134006 (Lot serial: Device id #134003); Model Catalog: 134009 (Lot serial: Device id #134009); Model Catalog: 134006 (Lot serial: Device id #134009); Model Catalog: 134003 (Lot serial: Device id #134003); Model Catalog: 134009 (Lot serial: Device id #134003)