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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Ortho clinical diagnostics has received complaints of centrifuge buckets (part number 4412-r) disconnecting from their supports during centrifugation when using the hettich rotanta 46 rsc robotic centrifuges (models 4815 4816 and 4817) that may be configured with engen laboratory automation systems. centrifuge bucket disconnections may result in damage to the hettich centrifuge.