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.
데이터 추가 비고
원인
Kavo dental gmbh is recalling the '1.007.5158 battery pack rechargeable 6v-3600mah' used in the diagnodent 2095. kavo dental became aware that vibrations during transport and other external influences can lead to an internal electrical short-circuit of the battery pack. this can lead to overheating and therefore melting of the battery packs plastic case.