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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1)occluded tubing may cause medication not to be delivered. 2)misprogrammed infusion caused by ignoring the warning message. 3) specific esd protection circuitry may result in an over or under infusion. 4)certain fluids solidify in the pumping mechanism. 5) iui connector failure when they become corroded or contaminated.
Model Catalog: 8015 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8110 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8650 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8600 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8120 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8300 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8220 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8000APM (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8100LVP (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: 8210 (Lot serial: MORE THAN 10 SERIAL NUMBERS)