How many FDA warning letters has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. received?

Argus HQ has not recorded an FDA warning letter for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. in our current dataset.

What FDA recalls has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. issued?

Argus HQ has recorded 18 FDA recalls tied to PHILIPS MEDICAL SYSTEMS NEDERLAND B.V..

Is PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 18 recalls, and 0 approval records for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. Review the linked FDA source records directly before drawing a compliance conclusion.

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PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Name: FDA Enforcement Actions Against PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Creator: Argus HQ
License: https://argushq.ai/methodology

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_recall2026-06-24
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032…
fda_recall · device_recall2026-06-24
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 5M12, Model Numbers: 722227 with Software release R2.2.0, R2.2.…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 7M12, Model Numbers: 722078, 722223 with Software release R2.2.…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 7B12/12, Model Numbers: 722067, 722225 with Software release R2…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 5M20, Model Numbers: 722228 with Software release R2.2.0, R2.2.…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 7M20, Model Numbers: 722079, 722224 with Software release R2.2.…
fda_recall · device_recall2026-06-10
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 7B20/15, Model Numbers: 722068, 722226 with Software release R2…
fda_recall · device_recall2026-06-03
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063,…
fda_recall · device_recall2026-06-03
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003…
fda_recall · device_recall2026-05-27
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion systems not configured with an optional auxiliary pan handle. In…
fda_recall · device_recall2026-05-27
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Allura system; System Code Description (Model Numbers): Allura Xper FD10C (72200…
fda_recall · device_recall2026-05-27
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Integris-Allura system; System Code Description (Model Numbers): Integris CV Ces…
fda_recall · device_recall2026-05-27
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063),…
fda_recall · device_recall2026-05-20
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion. System Code Description (Model Number): Azurion 3 M12 (722221,…
fda_recall · device_recall2026-04-22
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips AneurysmFlow. Model Number: 001015. AneurysmFlow is a software medic…

Frequently asked questions

How many FDA warning letters has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. received?: Argus HQ has not recorded an FDA warning letter for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. in our current dataset.
What FDA recalls has PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. issued?: Argus HQ has recorded 18 FDA recalls tied to PHILIPS MEDICAL SYSTEMS NEDERLAND B.V..
Is PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 18 recalls, and 0 approval records for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.. 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.