Medtronic Neuromodulation Clinician Programmer Application (CPA) model A610 Clinician Software Application Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Clinician Programmer Application (CPA) model A610 Clinician Software Application
Brand
Medtronic Neuromodulation
Lot Codes / Batch Numbers
Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081
Products Sold
Clinician Programmer Application (CPA) model A610 version 3.0.1048, 3.0.1057, 3.0.1062, and 3.0.1081
Medtronic Neuromodulation is recalling Clinician Programmer Application (CPA) model A610 Clinician Software Application due to A software anomaly may occur with the clinician programmer application.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A software anomaly may occur with the clinician programmer application.
Recommended Action
Per FDA guidance
A customer letter was distributed to impacted customers beginning September 16, 2021. Customers are asked to contact their Medtronic representative or Medtronic Technical Services at 1-800-707-0933 to troubleshoot should they experience the software anomaly issue.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026