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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:184987

Medtronic Ares Antibiotic-Impregnated Catheter, REF: 91101, Sterile, Rx Only. Used in the treatment of hydrocephalus as a component of a shunt system when draining or shunting of cerebrospinal fluid (CSF) is indicated.

Official recall number

Z-0738-2021

Evidence summary

Product code
JXG
Recall status
Open, Classified
Event initiated
December 08, 2020
Root cause
Packaging change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0738-2021

Field note

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