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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Philips has discovered through customer feedback and internal testing a failure with the image disk causing the entire image processing chain to be blocked due to a software design error. this causes image data to be lost and eventually loss of live imaging functionality.
Model Catalog: ALLURA XPER FD20/10 (Lot serial: 53388068); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 54178388); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 57436105); Model Catalog: 000454 (Lot serial: 55114616); Model Catalog: ALLURA XPER FD10 (Lot serial: > 10 contact mfg.); Model Catalog: ALLURA XPER FD20/20 (Lot serial: 62544258); Model Catalog: ALLURA XPER FD20/20 (Lot serial: 53329363); Model Catalog: ALLURA XPER FD20 (Lot serial: > 10 contact mfg.); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 55104885); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 53772614)