FDA
Food and Drug Administration · Recall Z-2893-2026 · Jun 17, 2026Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The hazard
Potential Loss of imaging functionality, loss of motorized movement, or loss of data due to unauthorized Hard Disk Drives. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Philips Allura, Cardio Vascular-Allura Centron. Model Number: 722400. Interventional Fluoroscopic X-Ray System.
Affected identifiers
Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.
Model Model Number: 722400. UDI Number: (01)00884838042315(21)282Model (01)00884838042315(21)206Model (01)00884838042315(21)187Model (01)00884838042315(21)486Model (01)00884838042315(21)480Model (01)00884838042315(21)71Model (01)00884838042315(21)322Model (01)00884838042315(21)506Model (01)00884838042315(21)429Model (01)00884838042315(21)413Model (01)00884838042315(21)497Model (01)00884838042315(21)507Model (01)00884838042315(21)502Model (01)00884838042315(21)222Model (01)00884838042315(21)144Model (01)00884838042315(21)510Model (01)00884838042315(21)190Model (01)00884838042315(21)43Model (01)00884838042315(21)439Model (01)00884838042315(21)176Model (01)00884838042315(21)76Model (01)00884838042315(21)364Model (01)00884838042315(21)209Model (01)00884838042315(21)382Model (01)00884838042315(21)178UPC 00884838042315Would you have heard about this one?
RapidRecall watches everything you own against every new federal recall and emails you the moment something you bought turns up. Free for your most important items.
Start monitoring freeSourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.