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 access 1.0 ml insert cup used on unicel dxc synchron clinical systems might be the cause of some sample wheel motion errors when run using 13x100 sample tubes.
Model Catalog: 4773 (Lot serial: CUP LOT NUMBERS STARTING WITH); Model Catalog: 4772 (Lot serial: "09" OR LATER); Model Catalog: 4773 (Lot serial: "09" OR LATER); Model Catalog: 4772 (Lot serial: CUP LOT NUMBERS STARTING WITH); Model Catalog: 4767 (Lot serial: CUP LOT NUMBERS STARTING WITH); Model Catalog: 4767 (Lot serial: "09" OR LATER); Model Catalog: 4771 (Lot serial: "09" OR LATER); Model Catalog: 4771 (Lot serial: CUP LOT NUMBERS STARTING WITH); Model Catalog: 4768 (Lot serial: "09" OR LATER); Model Catalog: 4768 (Lot serial: CUP LOT NUMBERS STARTING WITH)