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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:128103

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, Catalog No. 46917. Intended to allow drainage and measurement of cerebrospinal fluid (CSF) and other fluids of similar physical character from the ventricles or the lumbar subarachnoid (intrathecal) region.

Official recall number

Z-1924-2014

Evidence summary

Product code
JXG
Recall status
Terminated
Event initiated
June 09, 2014
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1924-2014