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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.

Class II
Recalling firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Reason for recall
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
Affected products (lot / model / serial)
All codes
Distribution pattern
US and ROW.
Firm location
Best, Netherlands
Recall type
FDA Mandated
Product type
Devices
Status
Ongoing
Recall number
Z-2411-2026
Recall initiated
May 18, 2026
FDA classification date
June 16, 2026
FDA report date
June 24, 2026
FDA event ID
99223
Last updated on HTM Vibe
July 23, 2026
View on openFDA