Skip to content

DigitalDiagnost 712226Recalls & reported problems

Philips Medical Systems DMC GmbH · Solid State X-Ray Imager (Flat Panel/Digital Imager) · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Sep 21, 2023Open, Classified

    Potential for units suspended on the ceiling to fail and fall.

    Z-0274-2024 · Root cause: Under Investigation by firm · FDA record ↗

Other Solid state x-ray imager (flat panel/digital imager) devices

All Solid state x-ray imager (flat panel/digital imager) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.