FDAHealthMay 18, 2026

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. — Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Dete

⚠️ 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

Is this relevant to me?

Geography: US
Source agency: FDA
Category: Health
Published: May 18, 2026

US and ROW.

What's affected?

Product: Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost Eleva; Model # 708034 for MultiDiagnost Eleva with Flat Detector; Model # 708036 for MultiDiagnost Eleva; Model # 708037 for MultiDiagnost Eleva with Flat Detector; Model # 708038 for MultiDiagnost Eleva with Flat Detector.
Brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Lot code: All codes

Additional details

All codes

What should I do?

Recommended action

Class II recall. FDA Mandated

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.