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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Manufacturer has discovered that pump channel was placed in the incorrect slot during servicing the label on the channel does not control the functionality of the channel potenial for incorrect medication.
Model Catalog: DNM8153 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8163R (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8163 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8153R (Lot serial: ALL SERIAL NUMBERS); Model Catalog: 2M8153 (Lot serial: ALL SERIAL NUMBERS); Model Catalog: DNM 8153R (Lot serial: ALL SERIAL NUMBERS)