Reported Apr 8, 2026 · Ongoing

ALLURA Xper FD10/10; System Code: (1) 722005, (2)722011, (3)722027;

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 FD10/10
  • System Code
    • (1) 722005
    • (2)722011
    • (3)722027
Lot codes and dates
  • (1)
  • System Code722005
  • UDIN/A
  • System Serial Number

    113 of 113 codes

    • 321
    • 285
    • 490
    • 51
    • 298
    • 329
    • 49
    • 361
    • 323
    • 355
    • 456
    • 316
    • 169
    • 305
    • 565
    • 419
    • 269
    • 258
    • 346
    • 474
    • 497
    • 530
    • 261
    • 523
    • 384
    • 388
    • 271
    • 233
    • 367
    • 270
    • 427
    • 343
    • 399
    • 360
    • 212
    • 251
    • 112
    • 520
    • 70
    • 392
    • 128
    • 357
    • 485
    • 405
    • 306
    • 307
    • 467
    • 234
    • 287
    • 333
    • 533
    • 209
    • 369
    • 543
    • 332
    • 328
    • 366
    • 389
    • 538
    • 394
  • System Code722011
  • UDI00884838059047
  • System Serial Number

    176 of 176 codes

    • 49
    • 137
    • 375
    • 332
    • 102
    • 103
    • 95
    • 107
    • 380
    • 132
    • 171
    • 157
    • 270
    • 362
    • 76
    • 79
    • 22
    • 234
    • 308
    • 34
    • 324
    • 177
    • 84
    • 82
    • 319
    • 17
    • 133
    • 168
    • 345
    • 344
    • 83
    • 59
    • 15
    • 170
    • 163
    • 101
    • 255
    • 173
    • 325
    • 87
    • 155
    • 40
    • 154
    • 215
    • 273
    • 222
    • 203
    • 214
    • 220
    • 242
    • 166
    • 71
    • 156
    • 36
    • 186
    • 300
    • 213
    • 372
    • 41
    • 55
  • System Code722027
  • UDI00884838054196
  • System Serial Number

    273 of 273 codes

    • 351
    • 332
    • 1
    • 71
    • 319
    • 43
    • 101
    • 29
    • 50
    • 112
    • 240
    • 241
    • 175
    • 298
    • 280
    • 107
    • 183
    • 202
    • 164
    • 153
    • 335
    • 288
    • 342
    • 134
    • 156
    • 265
    • 306
    • 307
    • 152
    • 106
    • 169
    • 203
    • 234
    • 209
    • 267
    • 284
    • 263
    • 127
    • 116
    • 174
    • 39
    • 49
    • 56
    • 120
    • 123
    • 133
    • 305
    • 246
    • 255
    • 40
    • 178
    • 104
    • 42
    • 266
    • 187
    • 321
    • 328
    • 282
    • 184
    • 53
Amount recalled
112 units (138 US, 422 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, 6:30 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.