FDA recall record · openFDA

Philips Medical Systems DMC GmbH

6 FDA recalls on record (2025) — 6 device. 6 still ongoing.

Class I (most serious)

Class II

Class III

ongoing

How to read this. A recall count is not a quality verdict — large manufacturers recall more simply by volume, and a voluntary recall is the safety system working as intended. The signal to weight is the Class I count (the FDA's most-serious tier — reasonable probability of serious harm or death) and whether recalls are still ongoing. Most recalls are Class II/III. "Ongoing" reflects openFDA's last-published status — device recalls often stay marked ongoing long after they're resolved in practice; confirm current status at the FDA.

Most common reasons

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 6

Recalls

Radiography 7300 C; Model Number: 712037; Class II 2025-10-01 DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035; Class II 2025-10-01 Precision CRF; Model Number: 706400; Class II 2025-10-01 ProxiDiagnost N90; Model Number: 706110; Class II 2025-10-01 CombiDiagnost R90; Model Number: 709031; Class II 2025-10-01 DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032; Class II 2025-10-01

RECORDED — these are the FDA's published recall enforcement records (openFDA). Recalls are listed under the exact firm name as filed; a large manufacturer may also file under name variants, so this may not be the company's complete cross-variant record — confirm at the FDA recall database. This page informs and routes; it is not medical advice or a verdict on the company.

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