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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A discrepancy between rf values when compared to who 64/002 an overestimation of rf vales by approximately 50% may be observed when used to calibrate n latex rf assays.
Model Catalog: OQDC13 (Lot serial: 183834 TO 18836A); Model Catalog: OQKZ13 (Lot serial: 199551 TO 199553B); Model Catalog: OQDB13 (Lot serial: 183834 TO 18836A); Model Catalog: OQKZ13 (Lot serial: 199451 TO 199453A)