Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:117850

2008 MeDS Pump, Venofer(R) Pump Product Usage: The 2008 MeDs pump is an optional accessory for use with the Fresenius 2008 Series Hemodialysis Machines and is intended to administer Venofer to treat iron deficiency anemia in patients with chronic kidney disease undergoing hemodialysis, where Venofer, in conjunction with hemodialysis, is prescribed by a physician.

Official recall number

Z-2082-2013

Evidence summary

Product code
KDI
Recall status
Terminated
Event initiated
April 01, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2082-2013

Field note

Send feedback

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