FDA Enforcement Class I Terminated

Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914. 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.

Recall: Z-1921-2014 · Reported July 9, 2014

Enforcement

Recall Number
Z-1921-2014
Event ID
68503
Classification
Class I
Status
Terminated
Product Type
Devices
Firm
Medtronic Neurosurgery
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
July 9, 2014
Initiation Date
June 9, 2014
Classification Date
June 27, 2014
Termination Date
January 14, 2015
Address
125 Cremona Dr, Goleta, CA, 93117-3083, United States

Description

Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914. 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.

Code Info

Lot No. 206843112 206854300 206875578 206923218 206951123 206962974 206986677 207167084 207246210 207312741 207441171 207466011 207466012 207560684 207632971 207659577 207716835 207716836 207766493 207900255 207945036 207983301 208008802

Distribution

Worldwide Distribution -- USA, Australia, Belgium, Canada, Croatia, Cyprus, Denmark, Egypt, Finland, France, Greece, Iran, Israel, Italy, Kuwait, Netherlands, Norway, Poland, Puerto Rico, Romania, Russian Federation, Saudi Arabia, Singapore, South Africa, Switzerland, Turkey, and United Kingdom.

Quantity

5,744 units