Medtronic Neuromodulation vs Philips North America: FDA Enforcement Comparison

Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 36 for Medtronic Neuromodulation.

Medtronic Neuromodulation: 0 warning letters, 36 recalls, 0 approval records, 0 Form 483s.

Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.

Side by side

Medtronic Neuromodulation — Warning letters0

Philips North America — Warning letters0

Medtronic Neuromodulation — Recalls36

Philips North America — Recalls355

Medtronic Neuromodulation — Approval records0

Philips North America — Approval records0

Medtronic Neuromodulation — Form 483s0

Philips North America — Form 483s0

Timeline

Medtronic Neuromodulation

Most recent FDA action: June 3, 2026

Full history →

Philips North America

Most recent FDA action: July 1, 2026

Full history →

Cite this comparison

Pre-formatted for a story, footnote, or reference list:

"Medtronic Neuromodulation vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 30, 2026. https://argushq.ai/compare/medtronic-neuromodulation-vs-philips-north-america

Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗