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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During routine bioburden testing [november 10th to 20th 2017] stryker found that the levels of bioburden were higher than our internal acceptable rates. therefore stryker is initiating this voluntary recall as the sterility of the product cannot be confirmed.
ADVANCED CEMENT MIXING BOWL EMPTY CEMENT CARTRIDGE NOZZLE AND PRESSURIZER;STRYKER AUTOPLEX SYSTEM WITHOUT NEEDLES AND CEMENT;PROX PRESS;INTRAMEDULLARY BRUSHES - DISPOSABLE