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 healthcare has discovered through customer complaints and internal testing an intermittent electronic product defect in accordance with health canada safety code 20a and some provincial regulations. in certain circumstances a software error can lead to a situation where the five minute fluoroscopy audible signal does not sound as required in health canada safety code 20a and some provincial regulations. no injuries attributed to the problem are reported.
Model Catalog: 000454 (Lot serial: 33); Model Catalog: 000454 (Lot serial: 146); Model Catalog: ALLURA XPER FD20/20 (Lot serial: 607); Model Catalog: ALLURA XPER FD20/20 (Lot serial: 171); Model Catalog: ALLURA XPER FD20/20 (Lot serial: 97); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 154); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 215); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 40); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 489); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 405); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 449); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 306); Model Catalog: ALLURA XPER FD10/10 (Lot serial: 307); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 168); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 567); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 283); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 57); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 52); Model Catalog: ALLURA XPER FD20/10 (Lot serial: 37); Model Catalog: ALLURA XPER FD