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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Siemens is conducting a field corrective action for the advia centaur and advia centaur xp immunoassay systems fluid reservoir connector tubing. the tubing for the wash 1 acid and base bottle reservoirs may be affected. on some systems a slight cracking of the tubing at the connecting fitting on the reservoir connector assembly may occur due to mechanical stress and may result in a minor drip of fluid onto the reservoir and into the drip tray located underneath the reservoirs. the drip will cause the reservoir to empty faster than the system expects.