FDA Device recall Z-1151-2024
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems
- FDA Device
- Class II
- ongoing
- Published 2024-02-28
On 2024-02-28 the FDA classified a Class II recall of Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems by Philips Medical Systems Nederland B V, citing disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1151-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-01-02 |
| Published | 2024-02-28 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Medical Systems Nederland B V |
| Distribution | US |
Product
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the Disk Bay of the PC component of affected systems. Affected PCs: Imaging Processing PC, Host PC, FlexVision PC Allura Xper Model Name - Model Number: Allura Xper FD10 722003 722010 722026; Allura Xper FD10 OR Table 722022; Allura Xper FD10/10 722005 722011 722027; Allura Xper FD10C 722001; Allura Xper FD20 722006 722012 722028; Allura Xper FD20 Biplane 722008 722013; Allura Xper FD20 Biplane OR Table 722025; Allura Xper FD20 OR Table 722023 722035; Allura Xper FD20/10 722029; Allura Xper FD20/15 722058; Allura Xper FD20/15 OR Table 722059; Allura Xper FD20/20 722038; Allura Xper FD20/20 OR Table 722039; (Allura Centron - 722400 is impacted by this recall, but Allura Centron systems are not distributed in the United States.)
Reason
Disk Bay may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
Identifiers
| code_info | Allura Xper FD10 722003 - no UDI Serial Numbers 1031 105 1074 1114 1181 1187 1209 1311 1349 1435 1472 1529 1555 1594 17…Allura Xper FD10 722003 - no UDI Serial Numbers 1031 105 1074 1114 1181 1187 1209 1311 1349 1435 1472 1529 1555 1594 1700 1719 1788 268 283 285 368 390 445 467 472 482 485 690 906 912 913 928 940 , 722010 - UDI-DI 00884838059030 or 00884838059191, some units do not have UDI Serial Numbers 1005 1009 1011 1025 1028 1040 1041 1042 1043 1048 1064 1069 107 1078 1082 1084 1108 1109 1112 1118 1123 1126 1128 1132 1144 1149 1170 1173 1176 1181 1183 1209 1210 1214 1226 1230 1233 1234 1235 1236 1244 1261 1263 1275 1279 1283 1287 1292 1297 1298 1302 1308 1309 1310 1312 1328 133 1336 1344 1347 1365 1369 1370 1373 1391 1395 1396 1397 1398 1424 1425 1428 1432 1436 1440 1441 1442 145 158 170 175 177 190 191 209 214 215 218 227 241 244 252 280 281 285 286 290 314 327 33 337 343 344 359 360 365 38 39 40 414 42 422 423 43 453 467 468 477 478 479 480 485 488 500 505 521 527 531 567 572 585 592 604 605 609 61 611 624 636 637 638 641 646 648 65 651 656 662 667 668 670 671 673 675 677 679 68 683 690 693 694 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1151-2024%22
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