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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Philips can no longer service or replace the mpt7-4 transesophageal echocardiograph (tee) transducer and in particular philips can no longer procure a key service part of the transducer and the performance of this part may degrade with time and use leading to a reduction in the range of articulation of the transducer. philips is providing customers with a field safety notice to notify customers of the issue and provide philips' current general recommendations for testing and operational procedures for tee transducers.