Medtronic Perfusion Systems 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 54 for Medtronic Perfusion Systems.

Medtronic Perfusion Systems: 0 warning letters, 54 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 Perfusion Systems — Warning letters0

Philips North America — Warning letters0

Medtronic Perfusion Systems — Recalls54

Philips North America — Recalls355

Medtronic Perfusion Systems — Approval records0

Philips North America — Approval records0

Medtronic Perfusion Systems — Form 483s0

Philips North America — Form 483s0

Timeline

Medtronic Perfusion Systems

Most recent FDA action: August 5, 2026

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Philips North America

Most recent FDA action: July 1, 2026

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Cite this comparison

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

"Medtronic Perfusion Systems vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/medtronic-perfusion-systems-vs-philips-north-america

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