Medtronic Neuromodulation: Medical Device Recall in 2021 - (Recall #: Z-0201-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2021.

Data Source: FDA.

Product Description:

Clinician Programmer Application (CPA) model A610 Clinician Software Application

Product Classification:

Class II

Date Initiated: September 23, 2021

Date Posted: November 10, 2021

Recall Number: Z-0201-2022

Event ID: 88761

Reason for Recall:

A software anomaly may occur with the clinician programmer application.

Status: Ongoing

Product Quantity: 3302

Code Information:

Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081

Distribution Pattern:

Worldwide distribution - US Nationwide distribution and the countries of Australia, New Zealand, Canada, Europe, India, Japan, Korea, Middle East, Latin America, Africa, SE Asia and China.

Voluntary or Mandated:

Voluntary: Firm initiated