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Philips Allura under the following System Descriptions and corresponding model numbers: 1. Allura Xper FD10; Model Numbers: 722003, 722010, 722026. 2. Allura Xper FD10 OR Table; Model Number: 722033. 3. Allura Xper FD10/10; Model Numbers: 722005, 722011, 722027. 4. Allura Xper FD10C; Model Number: 722001. 5. Allura Xper FD20; Model Numbers: 722006, 722012, 722028. 6. Allura Xper FD20 Biplane; Model Numbers: 722008, 722013. 7. Allura Xper FD20 Biplane OR Table; Model Number: 722025. 8. Allura Xper FD20 OR Table; Model Numbers: 722015, 722023, 722035. 9. Allura Xper FD20/10; Model Number: 722029. 10. Allura Xper FD20/15; Model Number: 722058. 11. Allura Xper FD20/15 OR Table; Model Number: 722059. 12. Allura Xper FD20/20; Model Number: 722038. 13. Allura Xper FD20/20 OR Table; Model Number: 722039. 14. Allura Xper R9 7 M12; Model Number: 722065. 15. Allura Xper R9 7 M20; Model Number: 722066. 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)
1. Allura Xper FD10; Model Numbers (UDI Numbers): 722003 (N/A), 722010 ((01)00884838059030(21)754, (01)00884838059030(21)42, (01)00884838059030(21)500, (01)00884838059030(21)68, (01)00884838059030(21)521, (01)00884838059030(21)33, (01)00884838059030(21)1025, (01)00884838059030(21)668, (01)00884838059030(21)585, (01)00884838059030(21)641, (01)00884838059030(21)968, (01)00884838059030(21)890, (01)00884838059030(21)780, (01)00884838059030(21)667, (01)00884838059030(21)1279, (01)00884838059030(21)344, (01)00884838059030(21)359, (01)00884838059030(21)423, (01)00884838059030(21)1040, (01)00884838059030(21)478, (01)00884838059030(21)215, (01)00884838059030(21)1298, (01)00884838059030(21)970, (01)00884838059030(21)1226, (01)00884838059030(21)365, (01)00884838059030(21)1328, (01)00884838059030(21)1292, (01)00884838059030(21)1275, (01)00884838059030(21)755, (01)00884838059030(21)671, (01)00884838059030(21)677, (01)00884838059030(21)61, (01)00884838059030(21)477, (01)00884838059030(21)1078, (01)00884838059030(21)327, (01)00884838059030(21)65, (01)00884838059030(21)1369, (01)00884838059030(21)792, (01)00884838059030(21)679, (01)00884838059030(21)479, (01)00884838059030(21)485, (01)00884838059030(21)592, (01)00884838059030(21)229, (01)00884838059030(21)119, (01)00884838059030(21)662, (01)00884838059030(21)1235, (01)00884838059030(21)1214, (01)00884838059030(21)764, (01)00884838059030(21)902, (01)00884838059030(21)1344, (01)00884838059030(21)675, (01)00884838059030(21)191, (01)00884838059030(21)937, (01)00884838059030(21)1432, (01)00884838059030(21)308, (01)00884838059030(21)833, (01)00884838059030(21)1310, (01)00884838059030(21)728, (01)00884838059030(21)791, (01)00884838059030(21)987, (01)00884838059030(21)986, (01)00884838059030(21)1005, (01)00884838059030(21)1425, (01)00884838059030(21)965, (01)00884838059030(21)1132, (01)00884838059030(21)468, (01)00884838059030(21)527, (01)00884838059030(21)1442, (01)00884838059030(21)646, (01)00884838059030(21)648, (01)00884838059030(21)873, (01)00884838059030(21)274, (01)00884838059030(21)1391, (01)00884838059030(21)838, (01)00884838059030(21)999, (01)00884838059030(21)821, (01)00884838059030(21)170, (01)00884838059030(21)673, (01)00884838059030(21)683, (01)00884838059030(21)637, (01)00884838059030(21)784, (01)00884838059030(21)314, (01)00884838059030(21)1297, (01)00884838059030(21)638, (01)00884838059030(21)1112, (01)00884838059030(21)1373, (01)00884838059030(21)878, (01)00884838059030(21)1108, (01)00884838059030(21)830, (01)00884838059030(21)40, (01)00884838059030(21)39, (01)00884838059030(21)777, (01)00884838059030(21)608, (01)00884838059030(21)1260, (01)00884838059030(21)1052, (01)00884838059030(21)339, (01)00884838059030(21)447, (01)00884838059030(21)1250, (01)00884838059030(21)1147, (01)00884838059030(21)1034, (01)00884838059030(21)1421, (01)00884838059030(21)1258, (01)00884838059030(21)484, (01)00884838059030(21)626, (01)00884838059030(21)1332, (01)00884838059030(21)534, (01)00884838059030(21)868, (01)00884838059030(21)782, (01)00884838059030(21)985, (01)00884838059030(21)697, (01)00884838059030(21)707, (01)00884838059030(21)708, (01)00884838059030(21)1146, (01)00884838059030(21)1267, (01)00884838059030(21)891, (01)00884838059030(21)566, (01)00884838059030(21)569, (01)00884838059030(21)861, (01)00884838059030(21)1321, (01)00884838059030(21)1096, (01)00884838059030(21)906, (01)00884838059030(21)1366, (01)00884838059030(21)661, (01)00884838059030(21)872, (01)00884838059030(21)374, (01)00884838059030(21)243, (01)00884838059030(21)1428, (01)00884838059030(21)225, (01)00884838059030(21)812, (01)00884838059030(21)857, (01)00884838059030(21)1274, (01)00884838059030(21)598, (01)00884838059030(21)555, (01)00884838059030(21)844, (01)00884838059030(21)1285, (01)00884838059030(21)969, (01)00884838059030(21)1046, (01)00884838059030(21)1045, (01)00884838059030(21)31, (01)00884838059030(21)139, (01)00884838059030(21)928, (01)00884838059030(21)578, (01)00884838059030(21)1185, (01)00884838059030(21)28, (01)00
Units affected
5,012 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-2891-2026
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