FDAApril 24, 2019device

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-...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

boston scientific neuromodulationbostonboston scientific

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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