Medtronic Neuromodulation: Medical Device Recall in 2024 - (Recall #: Z-0780-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Model A710 Intellis Clinician Programmer Application, version 2.0.97

Product Classification:

Class II

Date Initiated: December 19, 2023

Date Posted: January 31, 2024

Recall Number: Z-0780-2024

Event ID: 93714

Reason for Recall:

Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.

Status: Ongoing

Product Quantity: 1 tablet

Code Information:

UDI/DI 00763000520076, S/N: NPL1000519

Distribution Pattern:

Germany

Voluntary or Mandated:

Voluntary: Firm initiated