Medtronic Neuromodulation: Medical Device Recall in 2025 - (Recall #: Z-1506-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.

Product Classification:

Class II

Date Initiated: January 9, 2025

Date Posted: April 9, 2025

Recall Number: Z-1506-2025

Event ID: 96237

Reason for Recall:

Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.

Status: Ongoing

Product Quantity: 4365 units

Code Information:

version v.2x, UDI/DI 00763000632793

Distribution Pattern:

Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canary Islands, Czech Republic, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, Portugal, Puerto Rico, Spain, Sweden, Switzerland, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated