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 current labelling claim states "not made with natural rubber latex" which needs to be updated based on recent awareness that natural latex was used as a base ingredient in the early-stage manufacturing process which reduces the allergic protein found in natural latex. the overall risk to patients and consumers is remote for potential non-serious allergic reactions and unlikely for serious allergic reactions.