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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원인
Ohmeda has initiated a recall on these devices for unintended movement of the elevating base without user activating the footswitch.
Model Catalog: OMNIBED (Lot serial: THAN 54000.); Model Catalog: OMNIBED (Lot serial: HDGFVVVVV WHERE VVVVV IS LESS); Model Catalog: OMNIBED (Lot serial: HDGDVVVVV HDGEVVVVV); Model Catalog: (Lot serial: VVVVV IS LESS THAN 54000.); Model Catalog: (Lot serial: HDHEVVVVV HDHFVVVVV WHERE)