Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:205901

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter, REF 46915, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.

Official recall number

Z-1164-2024

Evidence summary

Product code
PCB
Recall status
Open, Classified
Event initiated
January 22, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1164-2024

Field note

Send feedback

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