RecallRadar

FDA Device recall Z-1920-2014

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

On 2014-07-09 the FDA classified a Class I recall of Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Catalog No. 46913 by Medtronic Neurosurgery, citing medtronic Neurosurgery is recalling the Medtronic Duet External Drainage and Monitoring Systems because the patient line tubing in the Duet External Drainage and Monitoring System….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1920-2014
ClassificationClass I
Statusterminated
Initiated2014-06-09
Published2014-07-09
Last updated2026-09-13 11:53 UTC
CompanyMedtronic Neurosurgery
DistributionPR

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

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.

Identifiers

code_info
Lot No. 206923217 207096627 207096630 207187691 207224897 207269986 207466017 207565424 207565425 207659575…Lot No. 206923217 207096627 207096630 207187691 207224897 207269986 207466017 207565424 207565425 207659575 207659576 207739874 207875274 207945037 207982847

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1920-2014%22

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