Device evidence

device-recall:cfres:152021

Fresenius 2008K@home Series : Hemodialysis System

Official recall number

Z-1029-2017

Evidence summary

Product code: KDI
Recall status: Terminated
Event initiated: December 21, 2016
Root cause: Device Design
Source snapshot: d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product: Z-1029-2017