Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:181125

EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F

Official recall number

Z-2209-2020

Evidence summary

Product code
MSD
Recall status
Terminated
Event initiated
June 14, 2019
Root cause
Error in labeling
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2209-2020

Field note

Send feedback

We'll only use this to respond to your feedback.