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Class I Medical Device Recall: Medtronic Neurologic Technologies, Innervision Snap Shunt Ventricular Catheter, BioGlide and Snap Shunt Ventricular Catheter, BioGlide

Published by CDRH Consumer News March 26th, 2009 in Regulatory Affairs

Reason for Recall: The ventricular catheter may become detached from the snap base assembly after implantation and may increase the need for emergency corrective surgery.

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