Philips North America vs RUBICON RESEARCH: FDA Enforcement Comparison

Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 2 for RUBICON RESEARCH.

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

RUBICON RESEARCH: 0 warning letters, 0 recalls, 2 approval records, 0 Form 483s.

Side by side

Philips North America — Warning letters0

RUBICON RESEARCH — Warning letters0

Philips North America — Recalls355

RUBICON RESEARCH — Recalls0

Philips North America — Approval records0

RUBICON RESEARCH — Approval records2

Philips North America — Form 483s0

RUBICON RESEARCH — Form 483s0

Timeline

Philips North America

Most recent FDA action: July 1, 2026

Full history →

RUBICON RESEARCH

Most recent FDA action: July 17, 2026

Full history →

Cite this comparison

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

"Philips North America vs RUBICON RESEARCH: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/philips-north-america-vs-rubicon-research

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