Medtronic Duet External Drainage and Monitoring System — Class I medical device recall Z-1920-2014

Terminated recall by Medtronic Neurosurgery, reported 2014-07-09, distributed in PR. Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems because the pa

Recall number	`Z-1920-2014`
Product type	Medical device
Classification	Class I
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Medtronic Neurosurgery, Goleta, CA, United States
Recall initiated	2014-06-09
Classified	2014-06-27
Reported by FDA	2014-07-09
Terminated	2015-01-14
Distributed	PR
Countries outside the US	AU, BE, CA, CH, CY, DK, EG, FI, FR, GB, GR, HR, IL, IR, IT, KW, NL, NO, PL, RO, SA, SG, TR, ZA
Quantity	3,026 units
Lot numbers	`206923217`, `207096627`, `207096630`, `207187691`, `207224897`, `207269986`, `207466017`, `207565424`, `207565425`, `207659575`, `207659576`, `207739874`, `207875274`, `207945037`, `207982847`
Model numbers	`46913`

Product

Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Catalog No. 46913. 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.

Reason for recall

Medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems because the patient line tubing in the Duet External Drainage and Monitoring Systems may become disconnected from the patient line stopcock.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1920-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.