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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Smiths medical has become aware of an increased trend in reports of "motor not running" ("mnr") and "motor rate error" ("mre") alarm message events with certain medfusion syringe infusion pumps models 3010a and 3500 ("pump"). these are high priority alarm messages which can occur for a variety of reasons as part of the usual self-test functionality of these pumps. the pump stops delivery when an mnr/mre alarm message event occurs.