Reported Apr 8, 2026 · Ongoing

ALLURA Xper FD20; System Code: (1) 722006, (2)722012, (3)722028;

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 FD20
  • System Code
    • (1) 722006
    • (2)722012
    • (3)722028
Lot codes and dates
  • (1)
  • System Code722006
  • UDIN/A
  • System Serial Number

    821 of 821 codes

    • 1706
    • 1730
    • 1936
    • 2250
    • 518
    • 1260
    • 1831
    • 1095
    • 1096
    • 1370
    • 1564
    • 2269
    • 471
    • 1293
    • 1762
    • 1764
    • 225
    • 1832
    • 204
    • 1818
    • 778
    • 2587
    • 1092
    • 1273
    • 2274
    • 2569
    • 1425
    • 1496
    • 707
    • 1448
    • 1466
    • 2183
    • 1502
    • 2201
    • 920
    • 1654
    • 1707
    • 1206
    • 637
    • 1326
    • 2152
    • 637220
    • 2536
    • 861
    • 172
    • 529
    • 1711
    • 1201
    • 1363
    • 2027
    • 2187
    • 730
    • 616
    • 550
    • 2336
    • 1407
    • 1259
    • 1913
    • 674
    • 1477
  • System Code722012
  • UDI00884838059054
  • System Serial Number

    1,886 of 1,886 codes

    • 481
    • 423
    • 1506
    • 1713
    • 1396
    • 2821
    • 828
    • 383
    • 2942
    • 2308
    • 1271
    • 613
    • 1945
    • 1281
    • 1188
    • 2323
    • 369
    • 160
    • 124
    • 848
    • 2265
    • 459
    • 469
    • 1120
    • 814
    • 815
    • 2610
    • 278
    • 297
    • 352
    • 511
    • 856
    • 560
    • 2522
    • 2735
    • 1645
    • 1407
    • 2924
    • 1608
    • 2707
    • 570
    • 1293
    • 424
    • 1047
    • 274
    • 2933
    • 135
    • 150
    • 2740
    • 336
    • 741
    • 1649
    • 2687
    • 655
    • 1192
    • 577
    • 578
    • 2203
    • 1036
    • 1063
  • System Code722028
  • UDI00884838054202
  • System Serial Number

    2,379 of 2,379 codes

    • 1756
    • 1569
    • 1956
    • 129
    • 1233
    • 2206
    • 1690
    • 928
    • 1774
    • 2502
    • 317
    • 869
    • 668
    • 1017
    • 406
    • 540
    • 548
    • 590
    • 596
    • 1957
    • 110
    • 2261
    • 173
    • 1310
    • 866
    • 1043
    • 466
    • 1077
    • 877
    • 896
    • 987
    • 995
    • 1343
    • 1439
    • 895
    • 265
    • 305
    • 1154
    • 1000
    • 1909
    • 121
    • 1716
    • 1983
    • 2061
    • 784
    • 729
    • 1393
    • 1948
    • 525
    • 1656
    • 1461
    • 209
    • 825
    • 408
    • 570
    • 218
    • 734
    • 1050
    • 1751
    • 454
Amount recalled
5084 units (1616 US, 3468 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?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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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, 5:58 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.