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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Manufacturer's robotics process problem as extra energy was applied to the connector anchoring mechanism.
Model Catalog: SVVI103 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SD 200 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SVVI (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SVDD303 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SVDD300 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SVDD 300 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSVI103 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSVI100 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR306 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR303 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR300 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR203 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR200 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR 306 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR 303 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR 300 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SSR 200 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: SS103 (Lot serial: ALL SERIAL NUMBERS); Model C