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 screw plug of the battery compartment may be faulty on some oxylog 3000 plus units produced bewteen may and august 2017 with serial number ranges: aske-0001 to askh-0214. the material used for the screws indicate damage around the thread. this can result in the battery compartment not closing properly.