Brand

Medtronic Neuromodulation: official recall notices

6 official recall or safety notices published on this site name Medtronic Neuromodulation, dated between 2023-06-06 and 2026-04-08. They were issued by 1 authority: US FDA — Medical Devices (6).

Countries where the notices were issued: United States (6).

Name as written in the notices: Medtronic Neuromodulation. This is the brand or the responsible company as each authority recorded it. A recall shows a safety system working; it is not a verdict on a brand. Follow the official notice for each product.

What this page counts: the notices published as pages on product-guru.org, over every date (this site publishes a selection of the notices in the ProductGuru index). The brand scorecards count every indexed notice in a rolling 24-month window instead, so their totals differ from this page.

Notices by year

Year	Notices
2026	1
2025	2
2023	3

Notices by authority

Authority	Notices
US FDA — Medical Devices	6

All notices

Date	Authority	Product	Hazard (as classified)
2026-04-08	US FDA — Medical Devices	Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following device	—
2025-11-20	US FDA — Medical Devices	Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT90	—
2025-04-03	US FDA — Medical Devices	Enhanced Verify Evaluation Handset (CFN HH90130FA)	—
2023-11-13	US FDA — Medical Devices	Medtronic SynchroMed II, Model 8637-20, Programmable pump	—
2023-11-13	US FDA — Medical Devices	Medtronic SynchroMed II, Model 8637-40, Programmable pump	—
2023-06-06	US FDA — Medical Devices	Vanta with AdaptiveStim Implantable Neurostimulator, Model 977006; spinal chord stimulation	—

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