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.
데이터 추가 비고
원인
The fine traction device is used to provide traction and enable fine adjustments to traction and orientation of the leg during orthopedic procedures. it is an accessory to the ot1000 series orthopedic surgical tables. steris has learned that the fine traction hand crank and rotation unlock button may lock up causing the fine traction adjustment of this accessory to be inoperable. steris has received no reports of illness or injuries one delay prior to the start of a procedure requiring the patient to be transferred to another surgical table to perform the procedure.