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.
데이터 추가 비고
원인
Within the framework of the continuous product observation of the market a potential malfunction of individual foot controls of the type s-n1/s-n2 was noticed.
Model Catalog: 05046200 (Lot serial: 01001 to 02318); Model Catalog: 30285000 (Lot serial: 22400 to 23429); Model Catalog: 05046200 (Lot serial: 22400 to 23429); Model Catalog: 05046210 (Lot serial: 22400 to 23429); Model Catalog: 06202400 (Lot serial: 22400 to 23429); Model Catalog: 06202400 (Lot serial: E01035 to E01071); Model Catalog: 05046210 (Lot serial: E01035 to E01071); Model Catalog: 05046200 (Lot serial: E01035 to E01071); Model Catalog: 30285000 (Lot serial: E01035 to E01071); Model Catalog: 06202400 (Lot serial: 01001 to 02318); Model Catalog: 05046210 (Lot serial: 01001 to 02318); Model Catalog: 30285000 (Lot serial: E02201 to E02485); Model Catalog: 30285000 (Lot serial: 01001 to 02318); Model Catalog: 06202400 (Lot serial: E01358 to E01658); Model Catalog: 05046210 (Lot serial: E01358 to E01658); Model Catalog: 05046200 (Lot serial: E01358 to E01658); Model Catalog: 30285000 (Lot serial: E01358 to E01658); Model Catalog: 06202400 (Lot serial: 24315 to 34040); Model Catalog: 05046210 (Lot seri