CareFusion 213, LLC 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 18 for CareFusion 213, LLC.

CareFusion 213, LLC: 1 warning letter, 17 recalls, 0 approval records, 0 Form 483s.

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

Side by side

CareFusion 213, LLC — Warning letters1

Philips North America — Warning letters0

CareFusion 213, LLC — Recalls17

Philips North America — Recalls355

CareFusion 213, LLC — Approval records0

Philips North America — Approval records0

CareFusion 213, LLC — Form 483s0

Philips North America — Form 483s0

Timeline

CareFusion 213, LLC

Most recent FDA action: July 22, 2026

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Philips North America

Most recent FDA action: July 1, 2026

Full history →

Cite this comparison

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

"CareFusion 213, LLC vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 27, 2026. https://argushq.ai/compare/carefusion-213-llc-vs-philips-north-america

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