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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Medline industries was informed of a recall of the bd needle 22g 1.5" safetyglide product code 301701. this needle is a component in several medline custom packs. bd issued the recall due to the presence of loose polypropylene foreign matter. this foreign matter has been identified as product hub material.