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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Complaints report that the 1ml safety glide needle disengages from the syringe after use. four scenarios have been reported: 1) the needle (cannula + hub) disengages after activating the safety feature (pop off) 2) the needle (cannula + hub) disengages from the syringe and remains on the patient's body after the procedure 3) the needle (cannula + hub) disengages when removing the needle cover 4) the needle (cannula + hub) disengages from the syringe and remains on the vial after drawing medication.