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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Certain liko uno patient lifts are being recalled because the actuator of the lift has the potential to separate when the upper arm is fully extended which may result in a patient fall.
Model Catalog: UNO 102 EM (Lot serial: 20001-21300); Model Catalog: UNO 102 (Lot serial: 20001-21300); Model Catalog: UNO 102 (Lot serial: 30001-48100); Model Catalog: UNO 102 EM (Lot serial: 30001-48100); Model Catalog: UNO 102 ES (Lot serial: 30001-48100); Model Catalog: UNO 102 EE (Lot serial: 30001-48100); Model Catalog: UNO 102 ES (Lot serial: 20001-21300); Model Catalog: UNO 102 EE (Lot serial: 20001-21300); Model Catalog: UNO 100 EE (Lot serial: 7090001-7096200); Model Catalog: UNO 100 EM (Lot serial: 7090001-7096200); Model Catalog: UNO 101 (Lot serial: 10001-11000)