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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At certain range of ablation depths a potential time-out error of the neuroblate system could occur when attempting to stop the laser probe at 5 to 7 mm from the bottom depth of the automatic or robotic probe driver.
Model Catalog: (Lot serial: C3561); Model Catalog: (Lot serial: C3567); Model Catalog: (Lot serial: C3000); Model Catalog: (Lot serial: C1497); Model Catalog: (Lot serial: C1177); Model Catalog: (Lot serial: C4855); Model Catalog: (Lot serial: C4860); Model Catalog: (Lot serial: C4863); Model Catalog: (Lot serial: C4843); Model Catalog: (Lot serial: C4746); Model Catalog: (Lot serial: C4741); Model Catalog: (Lot serial: C1813); Model Catalog: (Lot serial: C3980); Model Catalog: (Lot serial: C3573); Model Catalog: (Lot serial: C3003)