Official recall notice

FDA DeviceClass IINotable

FDA Recall: Philips MultiDiagnost Eleva with the following Model Numbers: Model # 708032 for MultiDiagnost El

Recall date
2026-06-24
FDA class
Class II

Why it was recalled

Hazard

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

Product description

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

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