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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Following receipt of customer complaints an investigation identified that a material change made by the supplier has resulted in capillary caps that are more difficult to apply to the capillaries. attempting to apply these capillary caps to the capillaries could result in spillage of the sample or possible breakage of the glass capillary. siemens is advising customers to use caution when applying the capillary caps with siemens multicap glass and multicap-s plastic capillaries to minimize the potential for breakage or bending.
Model Catalog: 10311053 (Lot serial: ALL LOTS MADE AFTER APRIL 2013); Model Catalog: 10311054 (Lot serial: ALL LOTS MADE AFTER APRIL 2013); Model Catalog: 10328655 (Lot serial: ALL LOTS MADE AFTER APRIL 2013)