Device evidence

device-recall:cfres:172011

McKesson Cardiology Hemo

Official recall number

Z-1490-2019

Evidence summary

Product code: DQK
Recall status: Terminated
Event initiated: March 25, 2019
Root cause: Software Design Change
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1490-2019