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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This recall is initiated due to a supplier manufacturing assembly defect with the right hand recline mechanism. use of this product may result in the loss of functionality of the three (3) position lock bar when in a recline position.
Model Catalog: 5570 (Lot serial: >10 contact the manufacturer); Model Catalog: 5251 (Lot serial: >10 contact the manufacturer); Model Catalog: 5261 (Lot serial: >10 contact the manufacturer); Model Catalog: 525S (Lot serial: >10 contact the manufacturer); Model Catalog: 529S (Lot serial: >10 contact the manufacturer); Model Catalog: 5271 (Lot serial: >10 contact the manufacturer); Model Catalog: 5281 (Lot serial: >10 contact the manufacturer); Model Catalog: 5291 (Lot serial: >10 contact the manufacturer); Model Catalog: 526S (Lot serial: >10 contact the manufacturer)