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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To further reduce the number of incidents associated with the alenti chair arjohuntleigh would like to re-iterate the important safety information. previous field safety correction actions reiterated the importance of following the instructions for use provided and included the introduction of a supplementary wall chart in the 2007 action. arjohuntleigh has revised the supplementary wall chart in april 2013. the changes include: 1. the correct instruction to not activate the alenti brake after the patient is removed from the bath tub. 2. the correct instruction to dry the patient inside the bath tub.