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Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.

Class II
Recalling firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Reason for recall
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives.
Affected products (lot / model / serial)
Model Number: 722400. UDI Number: (01)00884838042315(21)282, (01)00884838042315(21)206, (01)00884838042315(21)187, (01)00884838042315(21)486, (01)00884838042315(21)480, (01)00884838042315(21)71, (01)00884838042315(21)322, (01)00884838042315(21)506, (01)00884838042315(21)429, (01)00884838042315(21)413, (01)00884838042315(21)497, (01)00884838042315(21)507, (01)00884838042315(21)502, (01)00884838042315(21)222, (01)00884838042315(21)144, (01)00884838042315(21)510, (01)00884838042315(21)190, (01)00884838042315(21)43, (01)00884838042315(21)439, (01)00884838042315(21)176, (01)00884838042315(21)76, (01)00884838042315(21)364, (01)00884838042315(21)209, (01)00884838042315(21)382, (01)00884838042315(21)178, (01)00884838042315(21)243, (01)00884838042315(21)16, (01)00884838042315(21)110, (01)00884838042315(21)4, (01)00884838042315(21)101, (01)00884838042315(21)131, (01)00884838042315(21)93, (01)00884838042315(21)156, (01)00884838042315(21)347, (01)00884838042315(21)552, (01)00884838042315(21)482, (01)00884838042315(21)414, (01)00884838042315(21)80, (01)00884838042315(21)112, (01)00884838042315(21)42, (01)00884838042315(21)127, (01)00884838042315(21)407, (01)00884838042315(21)33, (01)00884838042315(21)184, (01)00884838042315(21)153, (01)00884838042315(21)189, (01)00884838042315(21)424, (01)00884838042315(21)201, (01)00884838042315(21)245, (01)00884838042315(21)122, (01)00884838042315(21)273, (01)00884838042315(21)228, (01)00884838042315(21)79, (01)00884838042315(21)307, (01)00884838042315(21)476, (01)00884838042315(21)108, (01)00884838042315(21)533, (01)00884838042315(21)250, (01)00884838042315(21)272, (01)00884838042315(21)252, (01)00884838042315(21)30, (01)00884838042315(21)308, (01)00884838042315(21)89, (01)00884838042315(21)525, (01)00884838042315(21)519, (01)00884838042315(21)148, (01)00884838042315(21)100, (01)00884838042315(21)258, (01)00884838042315(21)62, (01)00884838042315(21)22, (01)00884838042315(21)143, (01)00884838042315(21)49, (01)00884838042315(21)31, (01)00884838042315(21)363, (01)00884838042315(21)434, (01)00884838042315(21)70, (01)00884838042315(21)174, (01)00884838042315(21)137, (01)00884838042315(21)257, (01)00884838042315(21)232, (01)00884838042315(21)161, (01)00884838042315(21)471, (01)00884838042315(21)470, (01)00884838042315(21)155, (01)00884838042315(21)150, (01)00884838042315(21)136, (01)00884838042315(21)440, (01)00884838042315(21)545, (01)00884838042315(21)210, (01)00884838042315(21)279, (01)00884838042315(21)6, (01)00884838042315(21)149, (01)00884838042315(21)346, (01)00884838042315(21)317, (01)00884838042315(21)369, (01)00884838042315(21)348, (01)00884838042315(21)380, (01)00884838042315(21)61, (01)00884838042315(21)341, (01)00884838042315(21)438, (01)00884838042315(21)437, (01)00884838042315(21)77, (01)00884838042315(21)96, (01)00884838042315(21)513, (01)00884838042315(21)379, (01)00884838042315(21)355, (01)00884838042315(21)64, (01)00884838042315(21)12, (01)00884838042315(21)485, (01)00884838042315(21)503, (01)00884838042315(21)290, (01)00884838042315(21)168, (01)00884838042315(21)400, (01)00884838042315(21)283, (01)00884838042315(21)512, (01)00884838042315(21)236, (01)00884838042315(21)455, (01)00884838042315(21)173, (01)00884838042315(21)448, (01)00884838042315(21)92, (01)00884838042315(21)251, (01)00884838042315(21)139, (01)00884838042315(21)160, (01)00884838042315(21)109, (01)00884838042315(21)319, (01)00884838042315(21)68, (01)00884838042315(21)56, (01)00884838042315(21)199, (01)00884838042315(21)67, (01)00884838042315(21)233, (01)00884838042315(21)504, (01)00884838042315(21)535, (01)00884838042315(21)116, (01)00884838042315(21)27, (01)00884838042315(21)479, (01)00884838042315(21)423, (01)00884838042315(21)539, (01)00884838042315(21)285, (01)00884838042315(21)419, (01)00884838042315(21)305, (01)00884838042315(21)430, (01)00884838042315(21)449, (01)00884838042315(21)329, (01)00884838042315(21)472, (01)00884838042315(21)356, (01)00884838042315(21)292, (01)00884838042315(21)398, (01)00884838042315(21)230,
Units affected
257 units
Distribution pattern
US Nationwide distribution.
Firm location
Best, Netherlands
Recall type
Voluntary: Firm initiated
How the firm notified customers
Letter
Product type
Devices
Status
Ongoing
Recall number
Z-2893-2026
Recall initiated
June 17, 2026
FDA classification date
August 5, 2026
FDA report date
August 12, 2026
FDA event ID
99313
Last updated on HTM Vibe
August 18, 2026
View on openFDA