fda_recall · device_recall · high
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Class II recall: Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura…
- Event date
- 2026-06-24 00:00:00Z
- Observed
- 2026-07-09 22:52:08Z
- Source ID
- Z-2412-2026
- Payload hash
- 7d53be4765397344d06e2765…
Summary
Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection Status: Ongoing.
Informational only. Not legal, financial, or medical advice.

