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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Stryker medical has determined that the brake rod assemblies of the above referenced stretcher models that are built with a "5th wheel" series stretcher base were manufactured with roll pins that did not meet the material specifications. accordingly some roll pins may have fractured during the assembly process and could fall out of the brake rod assemblies rendering the brake or steer systems inoperable from certain pedals or causing a reduction in overall brake holding force.