Philips North America has been the subject of 355 FDA enforcement/approval records tracked by Argus HQ, compared to 1 for Oculus Technologies of Mexico, S.A. de C.V..
Oculus Technologies of Mexico, S.A. de C.V.: 0 warning letters, 1 recall, 0 approval records, 0 Form 483s.
Philips North America: 0 warning letters, 355 recalls, 0 approval records, 0 Form 483s.
Side by side
Oculus Technologies of Mexico, S.A. de C.V. — Warning letters0
Philips North America — Warning letters0
Oculus Technologies of Mexico, S.A. de C.V. — Recalls1
Philips North America — Recalls355
Oculus Technologies of Mexico, S.A. de C.V. — Approval records0
Philips North America — Approval records0
Oculus Technologies of Mexico, S.A. de C.V. — Form 483s0
Philips North America — Form 483s0
Timeline
Cite this comparison
Pre-formatted for a story, footnote, or reference list:
"Oculus Technologies of Mexico, S.A. de C.V. vs Philips North America: FDA Enforcement Comparison." Argus HQ, accessed August 29, 2026. https://argushq.ai/compare/oculus-technologies-of-mexico-s-a-de-c-v-vs-philips-north-america
Source: FDA.gov (aggregated across Warning Letters, Recalls, Approvals, Form 483s) ↗