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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Steris engineering analysis has determined the d1 pressure switch in the hydraulic column manifold does not adequately detect pressure level. if one or more of the table floor lock feet become unlocked due to the loss of hydraulic pressure there is a potential for the table hand control to incorrectly indicate that the floor lock feet are locked.