Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

LEAD 3387S-40 STIMLOC DBS Recalled by Medtronic Neuromodulation Due to There are a small number of units of...

Date: May 27, 2022
Company: Medtronic Neuromodulation
Status: Completed
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neuromodulation directly.

Affected Products

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

Quantity: 14 units

Why Was This Recalled?

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.

Where Was This Sold?

This product was distributed to 4 states: FL, MO, TX, WA

Affected (4 states)Not affected

About Medtronic Neuromodulation

Medtronic Neuromodulation has 95 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report