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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Hill-rom has become aware of a potential safety issue related to the slingbar 350 slingbar 360 slingbar wide 670 and sidebar standard which could be attached to various liko overhead and mobile lifts. a serious injury to a patient caregiver or bystander could result from tripping or otherwise falling in to the sling bar typically while the lift is parked or stored when not in use. the sling hook on the end of the sling bar could pierce a body structure such as the head shoulder or groin. the affected sling bar designs have not been sold or distributed since may 2008.