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 supplier w&h dentalwerk burmoos notified cbas of a potential malfunction in the foot control included in osscora surgical set (part# 91053). foot control may not switch back to zero position when pedal is released-causing motor to continue rotation. drilling mode not affected. automatic torque stop fully functional.