How many FDA warning letters has Medtronic Neuromodulation received?

Argus HQ has not recorded an FDA warning letter for Medtronic Neuromodulation in our current dataset.

What FDA recalls has Medtronic Neuromodulation issued?

Argus HQ has recorded 3 FDA recalls tied to Medtronic Neuromodulation.

Is Medtronic Neuromodulation FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Medtronic Neuromodulation. Review the linked FDA source records directly before drawing a compliance conclusion.

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Medtronic Neuromodulation

Name: FDA Enforcement Actions Against Medtronic Neuromodulation
Creator: Argus HQ
License: https://argushq.ai/methodology

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-06-03
Medtronic Neuromodulation — Class II recall: Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimul…
fda_recall · device_recall2026-06-03
Medtronic Neuromodulation — Class II recall: Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimul…
fda_recall · device_recall2026-05-20
Medtronic Neuromodulation — Class II recall: Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software App…

Frequently asked questions

How many FDA warning letters has Medtronic Neuromodulation received?: Argus HQ has not recorded an FDA warning letter for Medtronic Neuromodulation in our current dataset.
What FDA recalls has Medtronic Neuromodulation issued?: Argus HQ has recorded 3 FDA recalls tied to Medtronic Neuromodulation.
Is Medtronic Neuromodulation FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 3 recalls, and 0 approval records for Medtronic Neuromodulation. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.