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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Water from the humidifier ran into the housiong of the device. this cause a short circuit. no patient injury.
Model Catalog: (Lot serial: ARRH-0027/29/30/31/39/40/41/28); Model Catalog: (Lot serial: DEV LIC # 27340); Model Catalog: (Lot serial: ARRJ-0010/11/12/13/14/15/70); Model Catalog: (Lot serial: ARPN-0028); Model Catalog: (Lot serial: ARRF-0007/9)