Lower riskMedical device recall · FDA · Published December 19, 2023
Medtronic A710 Clinician Programmer App Version 2.0.97: Inability to Adjust Pain Therapy
Medtronic recalls its A710 Clinician Programmer Application version 2.0.97 due to potential inability to adjust pain therapy settings, risking inadequate or excessive treatment for patients.
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.
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Contact the company
📍Recalling firmMedtronic Neuromodulation7000 Central Ave Ne · Minneapolis, MN 55432-3568
✎ GovInfoNow plain-language explainer
Medtronic is recalling a specific version of its A710 Clinician Programmer Application because it may not properly connect with the patient's pain management device. This could lead to patients receiving incorrect pain treatment levels, potentially causing pain relief to be too low or too high. Read more at govinfonow.com/recall/56544-medtronic-a710-clinician-programmer-app-version-2-0-97-inability.
“Medtronic A710 Clinician Programmer App Version 2.0.97: Inability to Adjust Pain Therapy.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/56544-medtronic-a710-clinician-programmer-app-version-2-0-97-inability. Based on FDA recall #Z-0780-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0780-2024%22&limit=1).
The FDA announced on Dec. 19, 2023, that Medtronic Neuromodulation is recalling the Model A710 Intellis Clinician Programmer Application, version 2.0.97, due to a hazard where the software may fail to establish a session with an Implantable Neurostimulator. This failure can prevent clinicians from adjusting stimulation parameters, potentially leaving patients with inadequate or excessive therapy.
How to tell if you have it
Brand: Medtronic
Product: Model A710 Intellis Clinician Programmer Application, version 2.0.97
UDI/DI: 00763000520076
Serial Number: NPL1000519
The hazard
Medtronic discovered an instance where the Intellis A710 Clinician Programmer Application could no longer establish a session with the Implantable Neurostimulator. This resulted in the inability for the clinician to adjust stimulation parameters, meaning the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.
Context
GovInfoNow's records show Medtronic Neuromodulation has had 45 other recalls on record since Aug. 9, 2017. Other recent recalls of similar products include Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation (May 13, 2026) and Medtronic SynchroMed Flex Infusion Software Issue (April 8, 2026). A Dec. 3, 2025 recall cited a risk of prolonged surgery due to the Vanta CP App not functioning as intended.
How to tell if you have this one
Check if you have the A710 Clinician Programmer Application version 2.0.97. The software has a unique identifier (UDI/DI) of 00763000520076 and serial number NPL1000519.
Brand
Medtronic
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Software Version
Verify your software version is not 2.0.97 by checking the application settings or documentation.
How this recall unfolded
Recall timeline
FDA published this recall 43 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0780-2024 (December 19, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0780-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.