Data from New Zealand is current through July 2018. All of the data comes from the New Zealand Medicines and Medical Devices Safety Authority, 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 New Zealand.
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Recalling Organisation: Cass Medical Limited, 803 Paparata Road, Bombay, SOUTH AUCKLAND
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The unit is equipped with safety measures so no movement can occur without user interaction. during normal movements, however, isolated cases of overhead tube crane acceleration have been noticed.