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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Alcon has been informed by medtronic alcon's supplier of the devon light glove that medtronic is recalling specific lots of the devon light glove due to the potential for the glove to contain splits and holes. the devon light glove is included in specific builds of alcon custom-pak. based on the supplier information and recall initiated by the manufacturer of the devon light glove alcon has determined that the use of a torn/split light glove may pose a potential safety risk to the patient. due to the potential risk from using a torn/split devon light glove alcon is recalling all custom-paks built with the affected item.