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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Excessive strain may cause impairment of the interlocking between the arm joint and surgical light. inapropriate handling may cause a crack on the front pivot of the acrobat 2000 spring arm.
Model Catalog: ARD 567801093 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: ARD 567801094 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: ARD 567910901 (Lot serial: MORE THAN 10 SERIAL NUMBERS); Model Catalog: ARD 567910910 (Lot serial: MORE THAN 10 SERIAL NUMBERS)