FDAMarch 17, 2017device

DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and 3391/3391S, The lead kit contains one DBS lead in addition to multiple accessories used in DBS lead implant procedures. Among these accessories is the DBS lead holder, also referr...

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

The hazard

Medtronic received reports that the DBS depth stop did not adequately secure to the lead, which can result in DBS lead placement beyond the intended target.

What to do

FDA enforcement status: Terminated

Brands named

medtronic neuromodulationmedtronic

Recall history

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

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