Philips Medical Systems DMC GmbH — FDA Enforcement History

FDA action counts

Enforcement history

On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 71203…. On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number…. On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: Radiography 7300 C; Model Number: 712037;. On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: ProxiDiagnost N90; Model Number: 706110;. On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: CombiDiagnost R90; Model Number: 709031;. On 2025-11-19, Argus HQ recorded an FDA recall for Philips Medical Systems DMC GmbH, rated "high" severity in Argus HQ's classification: Philips Medical Systems DMC GmbH — Class II recall: Precision CRF; Model Number: 706400;. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed.

Risk pattern analysis

Argus HQ analysis — not an FDA finding

This section is Argus HQ analysis, not an FDA finding. Philips Medical Systems DMC GmbH has 6 separate FDA recalls on file, more than a single isolated recall event. A pattern across multiple FDA touchpoints does not by itself establish that any specific product currently poses a risk; it reflects only the frequency of FDA engagement with this company as recorded in Argus HQ's database. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures. This page reflects only the FDA event types Argus HQ currently tracks -- FDA Warning Letters, recalls, drug and biologic approvals, and Form 483 inspection observations -- and will update automatically as new FDA records are observed. Argus HQ does not independently verify FDA's underlying findings; this page summarizes what FDA has published and links back to the original FDA source for each event. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Frequently asked questions

What is the most recent FDA action on file for Philips Medical Systems DMC GmbH?

November 19, 2025. Argus HQ ingests new FDA enforcement records daily.

Has Philips Medical Systems DMC GmbH had product recalls?

Yes, 6 recalls on file. See the full history below for each one.

Is this FDA enforcement data for Philips Medical Systems DMC GmbH official?

Every record links directly to its primary FDA.gov source. Argus HQ aggregates and structures public FDA data; the verbatim FDA record is always the source of truth.

How many FDA actions has Philips Medical Systems DMC GmbH had?

Argus HQ has recorded 6 FDA events for Philips Medical Systems DMC GmbH: 0 warning letters, 6 recalls, 0 approvals, and 0 Form 483 inspection observations. Argus HQ ingests these records directly from FDA's own public enforcement and approval databases rather than from company disclosures.

Related enforcement actions

• Philips Medical Systems DMC GmbH — Class II recall: Precision CRF; Model Number: 706400; →
• Philips Medical Systems DMC GmbH — Class II recall: CombiDiagnost R90; Model Number: 709031; →
• Philips Medical Systems DMC GmbH — Class II recall: ProxiDiagnost N90; Model Number: 706110; →
• Philips Medical Systems DMC GmbH — Class II recall: Radiography 7300 C; Model Number: 712037; →
• Philips Medical Systems DMC GmbH — Class II recall: DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number… →
• Philips Medical Systems DMC GmbH — Class II recall: DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 71203… →

Compare with

• Philips Medical Systems DMC GmbH vs Philips North America
• Philips Medical Systems DMC GmbH vs Boston Scientific Corporation
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• Philips Medical Systems DMC GmbH vs Baxter Healthcare Corporation
• Philips Medical Systems DMC GmbH vs PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.