Reported Apr 8, 2026 · Ongoing

ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;

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 Biplane
  • System Code
    • (1) 722008
    • (2)722013
Lot codes and dates
  • (1)
  • System Code722008
  • UDIN/A
  • System Serial Number

    144 of 144 codes

    • 360
    • 361
    • 445
    • 296
    • 487
    • 390
    • 306
    • 178
    • 420
    • 267
    • 245
    • 2470
    • 491
    • 113
    • 386
    • 69
    • 413
    • 365
    • 454
    • 304
    • 442
    • 125
    • 441
    • 320
    • 325
    • 112
    • 254
    • 456
    • 52
    • 34
    • 239
    • 407
    • 187
    • 437
    • 82
    • 102
    • 288
    • 349
    • 106
    • 105
    • 481
    • 71
    • 424
    • 1236
    • 197
    • 264
    • 18
    • 19
    • 192
    • 124
    • 483
    • 244
    • 224
    • 470
    • 279
    • 141
    • 459
    • 357
    • 287
    • 116
  • System Code722013
  • UDI00884838059061
  • System Serial Number

    318 of 318 codes

    • 293
    • 424
    • 100
    • 174
    • 86
    • 83
    • 46
    • 170
    • 218
    • 441
    • 249
    • 639
    • 290
    • 153
    • 410
    • 1
    • 289
    • 518
    • 519
    • 626
    • 126
    • 141
    • 496
    • 379
    • 115
    • 42
    • 601
    • 214
    • 637
    • 360
    • 389
    • 303
    • 268
    • 264
    • 631
    • 254
    • 255
    • 515
    • 129
    • 15
    • 603
    • 278
    • 347
    • 426
    • 505
    • 109
    • 462
    • 149
    • 124
    • 216
    • 246
    • 84
    • 479
    • 69
    • 105
    • 638
    • 375
    • 531
    • 404
    • 575
Amount recalled
461 units (198 US, 263 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, 5:39 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.