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 the malleable shaft within 11/2 inches of the tip could cause failure of the hand tip. there is potential for injury to the patientfrom the disloged internal needle electrode. dk.
Model Catalog: 134006 (Lot serial: Device id #134003); Model Catalog: 134009 (Lot serial: Device id #134003); Model Catalog: 134003 (Lot serial: Device id #134006); Model Catalog: 134006 (Lot serial: Device id #134006); Model Catalog: 134003 (Lot serial: Device id #134003); Model Catalog: 134003 (Lot serial: device id #134009); Model Catalog: 134006 (Lot serial: device id #134009); Model Catalog: 134009 (Lot serial: device id #134009); Model Catalog: 134009 (Lot serial: Device id #134006)