Medtronic Neuromodulation: Medical Device Recall in 2023 - (Recall #: Z-2226-2023)

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:

A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

Product Classification:

Class II

Date Initiated: June 21, 2023

Date Posted: August 2, 2023

Recall Number: Z-2226-2023

Event ID: 92530

Reason for Recall:

When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.

Status: Ongoing

Product Quantity: 2 clinician tablets

Code Information:

Serial numbers NPL3011706 and NPL3016791, UDI-DI 643169738058.

Distribution Pattern:

International distribution to the countries of Israel and Serbia.

Voluntary or Mandated:

Voluntary: Firm initiated