fda_recall · device_recall · high
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0…
- Event date
- 2026-06-10 00:00:00Z
- Observed
- 2026-07-09 22:52:18Z
- Source ID
- Z-2284-2026
- Payload hash
- cb88225f071c4ce5ac42c587…
Summary
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoro… Status: Ongoing.
Informational only. Not legal, financial, or medical advice.