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.
데이터 추가 비고
Recalling Organisation: Law and Accounting Professional Trustees Limited, 336, Jackson Street, Petone
원인
The manufacturer advises that the product has been incorrectly labelled. the outer packaging is correct but inner packaging and product labelling is for size #30 obturators.