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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When the gamma camera detector #1 head is at a position directly above the patient table (relative 180 degree position) oil and/or grease contamination on the radius drive clutch (es) may result in non-user initiated drifting down of the gamma camera detector #1 head towards the patient table. patient injury may result if a patient is on the table and the downward drift is not detected in time to execute emergency patient removal.