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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When archiving task is stopped and then started in quick succession software defect causes incorrect study to be presented to radiologist while requested study gets erroneously deleted without being archived.
Model Catalog: HMI 11.9 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 11.8 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 4.5 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 4.6.1 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 5 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 11.0 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 11.5 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HMI 11.7 (Lot serial: ALL LOTS. CONTACT MFG); Model Catalog: HIM 11.6 (Lot serial: ALL LOTS. CONTACT MFG)