Philips Medical Systems Gmbh, DMC
Philips Medical Systems Gmbh, DMC has 5 FDA enforcement events on this register (33 product records) between 2018 and 2020: 5 device; the busiest year was 2018 with 3.
0% of its events are Class I; the most common class is Class II (5). 2 events are listed as ongoing; the recalling firm's address is in N/A.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 22 Jul 2020 | CombiDiagnost R90 Software Version R1.0 and R1.1 | Device | Class II | 1 | Ongoing |
| 19 Dec 2019 | CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic, general purpose. | Device | Class II | 2 | Ongoing |
| 7 Nov 2018 | Stationary Fluoroscopic X-ray System CombiDiagnost R90, Model 709030 Stationary Fluoroscopic X-ray System | Device | Class II | 1 | Terminated |
| 19 Sep 2018 | Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028, 712029, 712031, 712032701032, 712033, 712224, 712225, 712226, 712227, 712228. | Device | Class II | 1 | Terminated |
| 27 Jun 2018 | DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082 | Device | Class II | 28 | Terminated |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Philips Medical Systems Gmbh, DMC had?
5 enforcement events (33 product records) on this register, 2018–2020: 5 device.
Are any Philips Medical Systems Gmbh, DMC recalls ongoing?
2 events are listed as ongoing in the current openFDA export.
What class are Philips Medical Systems Gmbh, DMC recalls?
5 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.