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 recall is an extension of recall #30400 due to additional lots of the product have received additional complaint reports of pet ring coil breakage. could lead to bowl perforation or chronic enteric fistulas.
Model Catalog: 0010204 (Lot serial: 0010202: 43AOD*** TO 43IQD***); Model Catalog: 0010204 (Lot serial: 0010204: 43AOD*** TO 43IQD***); Model Catalog: 0010202 (Lot serial: 0010202: 43AOD*** TO 43IQD***); Model Catalog: 0010202 (Lot serial: 0010204: 43AOD*** TO 43IQD***)