PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: November 19, 2025 Initiated: October 6, 2025 #Z-0459-2026

Product Description

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

Reason for Recall

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).

Details

Recalling Firm
Abbott Medical
Units Affected
722 units
Distribution
Worldwide distribution.
Location
Plano, TX

Frequently Asked Questions

What product was recalled?
Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400. Recalled by Abbott Medical. Units affected: 722 units.
Why was this product 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).
Which agency issued this recall?
This recall was issued by the FDA Devices on November 19, 2025. Severity: Moderate. Recall number: Z-0459-2026.