company
Philips North America
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Evolution Upgrade 1.5T with MR Elastography (MRE). 1. Model Number (…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Evolution upgrade 3.0T with MR Elastography (MRE). 1. Model Number (…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips SmartPath to dStream for 1.5T with MR Elastography (MRE). 1. Model N…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF)…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model N…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips SmartPath to Ingenia Elition X with MR Elastography (MRE). 1. Model…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia Ambition S with MR Elastography (MRE). 1. Model Number (REF)…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Achieva 3.0T with MR Elastography (MRE). 1. Model Number (REF): 7812…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips SmartPath to dStream for XR and 3.0T with MR Elastography (MRE). 1.…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF)…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia 3.0T with MR Elastography (MRE). 1. Model Number (REF): 7813…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Achieva 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7811…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia 1.5T with MR Elastography (MRE). 1. Model Number (REF): 7813…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Achieva 1.5T Initial system with MR Elastography (MRE). 1. Model Num…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782120.…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia Elition S with MR Elastography (MRE). 1. Model Number (REF):…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia 3.0T CX with MR Elastography (MRE). 1. Model Number (REF): 7…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia 1.5T CX with MR Elastography (MRE). 1. Model Number (REF): 7…
- fda_recall · device_recall2026-05-06Philips North America — Class II recall: Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF):…
Frequently asked questions
- How many FDA warning letters has Philips North America received?
- Argus HQ has not recorded an FDA warning letter for Philips North America in our current dataset.
- What FDA recalls has Philips North America issued?
- Argus HQ has recorded 19 FDA recalls tied to Philips North America.
- Is Philips North America FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 19 recalls, and 0 approval records for Philips North America. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.