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.
데이터 추가 비고
원인
Philips' suresigns patient monitors vital signs monitors and vital signs viewers allow the device speaker volume to be adjusted by the user. philips healthcare has determined that in rare instances the continued use of these speakers at their maximum volume setting may result in the premature failure of the internal speaker. if the device speaker fails during use this may contribute to a delay in treatment of a patient.