Model A710 Intellis Clinician Programmer Application — Class II medical device recall Z-0780-2024
Ongoing recall by Medtronic Neuromodulation, reported 2024-01-31. Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) coul
| Recall number | Z-0780-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medtronic Neuromodulation, Minneapolis, MN, United States |
| Recall initiated | 2023-12-19 |
| Classified | 2024-01-22 |
| Reported by FDA | 2024-01-31 |
| Countries outside the US | DE |
| Quantity | 1 tablets |
| UPC / GTIN / UDI-DI | 00763000520076 |
| Model numbers | A710 |
Product
Model A710 Intellis Clinician Programmer Application, version 2.0.97
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0780-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.