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 healthcare diagnostics has received complaints for low recovery for magnesium (mg) quality control (qc) and patient samples following calibration of mg with dimension vista chem 1 cal lot 3gm081. investigation by siemens confirms that qc and patient samples show low recovery of mg by 0.25 mg/dl [0.10 mmol/l] across the assay range following calibration with 3gm081.