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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This recall has been initiated due to the potential that it was observed that creatinine rate blank method calibrator and control results were reporting values lower than target values indicated in the associated abx pentra multical n control and p control annexes. horiba has reassigned the target values and updated annexes for the products and lot numbers.