Medtronic Neuromodulation: Medical Device Recall in 2023 - (Recall #: Z-0217-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 27, 2022

Date Posted: November 8, 2023

Recall Number: Z-0217-2024

Event ID: 93170

Reason for Recall:

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.

Status: Completed

Product Quantity: 14 units

Code Information:

UDI/DI 00763000274320, Serial Number VA2JV2V

Distribution Pattern:

US: MO, FL, TX, WA

Voluntary or Mandated:

Voluntary: Firm initiated