FDAMay 27, 2022device

LEAD 3387S-40 STIMLOC DBS, Model Number 3387S-40. Electrical implantable device.

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

The hazard

There are a small number of units of the DBS Lead with StimLoc kit (3387S-40) due to a discrepancy in the Use By Date (UBD) printed on the outer packaged kit label versus the UBD printed on the individual product label.

What to do

FDA enforcement status: Completed

Brands named

medtronic neuromodulationmedtronic

UPCs

00763000274320

Recall history

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

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