Abbott Medical recalls Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400

Recall date

October 6, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0459-2026

FDA classification

Class II

Brand / firm

Abbott Medical

Sold / distributed

Worldwide distribution.

Why it was recalled

There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC).

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400