FDA
Food and Drug Administration · Recall Z-2928-2026 · Jun 29, 2026Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The hazard
Firmware issue potentially leading to loss of geometry movements. FDA Class II recall.
The remedy
Follow FDA guidance
About this recall
Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. 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 Numbers: 722026Model 722027Model 722028Model 722029Model 722035Model 722038Model 722039Model (01)00884838054202(21)1569Model (01)00884838059115(21)100Model (01)00884838059115(21)239Model (01)00884838054202(21)520Model (01)00884838054202(21)1956Model (01)00884838054189(21)683Model (01)00884838054196(21)351Model (01)00884838054202(21)129Model (01)00884838059115(21)305Model (01)00884838054196(21)332Model (01)00884838054202(21)1233Model (01)00884838054202(21)2206Model (01)00884838054202(21)1690Model (01)00884838054202(21)928Model (01)00884838054189(21)155Model (01)00884838054202(21)317Model (01)00884838054202(21)1774Model (01)00884838054202(21)2502UPC 00884838054202UPC 00884838059115UPC 00884838054189UPC 00884838054196Would you have heard about this one?
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