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.