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Recall Observatory FDA recall evidence

Device product

Fifty-five (55) cm 8 Contact Extension Kit, part number M365NM3138550 - Product Usage: The Deep Brain Stimulation (DBS) System is indicated for use in bilateral stimulation of the subthalamic nucleus (STN) as an adjunctive therapy in reducing some of the symptoms of moderate to advanced levodopa-responsive Parkinson s disease (PD) that are not adequately controlled with medication.

Z-2125-2020

April 24, 2019

Class II

Product summary

Firm
Boston Scientific Neuromodulation Corporation
Event
Event 84983
Status
Terminated
Classification
Class II
Quantity
8 units
Official record key
device-enforcement:Z-2125-2020

Official wording

Reason: The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.

Code information: Part number M365NM3138550; serial numbers 1049357, 1057232, 3014616, 1053194, 3010769, 3014631, 1057225 and 3012324.

Distribution pattern: Distributed OUS only. to 14 countries.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The firm is initiating a voluntary removal of certain spinal cord stimulation leads, lead extensions, adapters, and deep brain stimulation lead extensions due to the "use by date" displayed on the label which is later than the correct "use by date". No adverse health consequence is expected to occur from this issue.