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
Safety alert sent to all account re-emphasizing the proper way of loading the iv tubing in the pump so that proper flow will occur because of reported instances of free-flow.
Model Catalog: 2M8063 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8063E (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8064 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8064R (Lot serial: ALL SERIAL NUMBERS)