Medtronic Neuromodulation: Medical Device Recall in 2020 - (Recall #: Z-0612-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.

Product Classification:

Class II

Date Initiated: November 19, 2020

Date Posted: December 23, 2020

Recall Number: Z-0612-2021

Event ID: 86907

Reason for Recall:

A software anomaly in the A620 Patient Programmer application was identified that results in failure to connect with the Percept PC device.

Status: Terminated

Product Quantity: 12 devices

Code Information:

Model Number: B35200; GTIN: 00763000253363; Serial Numbers: NPI706941H, NPI707024H, NPI707000H, NPI706992H, NPI706963H, NPI706962H, NPI706987H, NPI706945H, NPI706952H, NPI706954H, NPI706955H, NPI706957H

Distribution Pattern:

US Nationwide distribution including in the states of Arizona, California, New Hampshire, Pennsylvania, Tennessee, Texas, Washington.

Voluntary or Mandated:

Voluntary: Firm initiated