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Philips Medical Systems DMC GmbH recalls

The FDA has posted 6 enforcement recalls from Philips Medical Systems DMC GmbH since 2025, none of them Class I (most serious). Most recent report: Nov 19, 2025.

Class II: 6
Class IIOngoingZ-0466-2026

Philips Medical Systems DMC GmbH recalls Radiography 7300 C

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e.…

  • Stationary X-Ray System
  • Device Design
Philips Medical System…Nov 19, 2025
Class IIOngoingZ-0463-2026

Philips Medical Systems DMC GmbH recalls Precision CRF

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e.…

  • Image-Intensified Fluoroscopic X-Ray System
  • Device Design
Philips Medical System…Nov 19, 2025
Class IIOngoingZ-0461-2026

Philips Medical Systems DMC GmbH recalls ProxiDiagnost N90

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e.…

  • Image-Intensified Fluoroscopic X-Ray System
  • Device Design
Philips Medical System…Nov 19, 2025
Class IIOngoingZ-0462-2026

Philips Medical Systems DMC GmbH recalls CombiDiagnost R90

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e.…

  • Image-Intensified Fluoroscopic X-Ray System
  • Device Design
Philips Medical System…Nov 19, 2025

Firm name as filed with the FDA: “Philips Medical Systems DMC GmbH”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.