Percussionaire Corporation vs Philips North America: FDA Enforcement Comparison

Philips North America has been the subject of 369 FDA enforcement/approval records tracked by Argus HQ, compared to 7 for Percussionaire Corporation.

Percussionaire Corporation: 0 warning letters, 7 recalls, 0 approval records, 0 Form 483s.

Philips North America: 0 warning letters, 369 recalls, 0 approval records, 0 Form 483s.

Side by side

Percussionaire Corporation — Warning letters0

Philips North America — Warning letters0

Percussionaire Corporation — Recalls7

Philips North America — Recalls369

Percussionaire Corporation — Approval records0

Philips North America — Approval records0

Percussionaire Corporation — Form 483s0

Philips North America — Form 483s0

Timeline

Percussionaire Corporation

Most recent FDA action: October 7, 2026

Full history →

Philips North America

Most recent FDA action: October 7, 2026

Full history →

Cite this comparison

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

"Percussionaire Corporation vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed October 13, 2026. https://argushq.ai/compare/percussionaire-corporation-vs-philips-north-america

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