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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In-house confirmation that a low percentage of filters were found to have a small residual matter within and around the filter. the residual matter is very small and could make its way to the patient.
Model Catalog: OL-618030-XX (Lot serial: see notice or contact mfr); Model Catalog: OL-609036-34 (Lot serial: see notice or contact mfr); Model Catalog: OL-040419-00 (Lot serial: see notice or contact mfr); Model Catalog: OL-040419-05 (Lot serial: see notice or contact mfr); Model Catalog: OL-544400-05 (Lot serial: see notice or contact mfr); Model Catalog: OL-608030-72 (Lot serial: see notice or contact mfr); Model Catalog: OL-608030-76 (Lot serial: see notice or contact mfr)