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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S.I.S.T.E.M.I srl are notifying their customers that they do not hold a device license for the seqex medical devices.
Model Catalog: HAND-HELD SPOT (Lot serial: CONTACT MANUFACTURER); Model Catalog: INTENSIVE PAD (Lot serial: CONTACT MANUFACTURER); Model Catalog: SMART (Lot serial: CONTACT MANUFACTURER); Model Catalog: FIELD INCREASERS (Lot serial: CONTACT MANUFACTURER); Model Catalog: MED (Lot serial: CONTACT MANUFACTURER); Model Catalog: FAM (Lot serial: CONTACT MANUFACTURER); Model Catalog: HC (Lot serial: CONTACT MANUFACTURER)