Reported Apr 8, 2026 · Ongoing

ALLURA Xper FD10; System Code: (1) 722003, (2)722010, (3)722026;

Philips Medical Systems Nederland B.v.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 6 · Best · N/A

Is this the product you have?

  • ALLURA Xper FD10
  • System Code
    • (1) 722003
    • (2)722010
    • (3)722026
Lot codes and dates
  • (1)
  • System Code722003
  • UDIN/A
  • System Serial Number

    447 of 447 codes

    • 445
    • 1555
    • 1084
    • 1411
    • 1232
    • 1259
    • 1023
    • 1947
    • 392
    • 1133
    • 1135
    • 1627
    • 746
    • 98
    • 1078
    • 367
    • 1584
    • 1599
    • 1153
    • 1154
    • 1032
    • 1694
    • 259
    • 1471
    • 1474
    • 684
    • 657
    • 385
    • 1551
    • 947
    • 1360
    • 1482
    • 1489
    • 177
    • 1634
    • 1663
    • 1704
    • 1214
    • 546
    • 1089
    • 305
    • 2936
    • 92
    • 1092
    • 1869
    • 119
    • 928
    • 1449
    • 1805
    • 998
    • 501
    • 503
    • 1114
    • 345
    • 1443
    • 1444
    • 8198
    • 63
    • 1189
    • 1954
  • System Code722010
  • UDI00884838059030
  • System Serial Number

    810 of 810 codes

    • 1123
    • 932
    • 239
    • 42
    • 360
    • 209
    • 500
    • 794
    • 921
    • 939
    • 286
    • 1440
    • 160
    • 1144
    • 521
    • 33
    • 107
    • 1025
    • 656
    • 668
    • 1261
    • 1170
    • 585
    • 364
    • 1128
    • 882
    • 499
    • 1230
    • 280
    • 488
    • 787
    • 968
    • 890
    • 780
    • 190
    • 1181
    • 694
    • 1279
    • 344
    • 1149
    • 423
    • 1176
    • 1173
    • 1040
    • 67
    • 1309
    • 763
    • 931
    • 306
    • 478
    • 240
    • 1298
    • 970
    • 1226
    • 290
    • 365
    • 651
    • 1275
    • 1292
    • 755
  • System Code722026
  • UDI00884838054189
  • System Serial Number

    1,036 of 1,036 codes

    • 683
    • 155
    • 1051
    • 1052
    • 618
    • 654
    • 786
    • 1132
    • 458
    • 1100
    • 770
    • 436
    • 1338
    • 1068
    • 233
    • 78
    • 432
    • 224
    • 1072
    • 796
    • 93
    • 543
    • 1248
    • 561
    • 1129
    • 781
    • 344
    • 374
    • 634
    • 908
    • 130
    • 370
    • 235
    • 190
    • 259
    • 323
    • 324
    • 969
    • 100
    • 98
    • 99
    • 142
    • 1246
    • 601
    • 877
    • 221
    • 204
    • 843
    • 1038
    • 1231
    • 114
    • 1287
    • 878
    • 558
    • 391
    • 633
    • 389
    • 1050
    • 1000
    • 909
Amount recalled
2291 units (493 US, 1798 OUS)

This recall covers 23 products

The agency filed one notice per product. You are reading one of them; the other 22 are below.

10 more are in the archive.

Where it was sold

  • Nationwide
  • GA

Why it was recalled

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:40 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.