Reported Apr 8, 2026 · Ongoing

Azurion 7 B20; System Code: (1)722068, (2)722226, (3)722236;

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?

  • Azurion 7 B20
  • System Code
    • (1)722068
    • (2)722226
    • (3)722236
Lot codes and dates
  • (1)
  • System Code722068
  • UDI00884838085367
  • System Serial Number

    421 of 421 codes

    • 547
    • 178
    • 467
    • 335
    • 147
    • 205
    • 170
    • 455
    • 494
    • 564
    • 418
    • 95
    • 440
    • 247
    • 225
    • 64
    • 149
    • 42
    • 153
    • 324
    • 323
    • 320
    • 85
    • 89
    • 109
    • 407
    • 239
    • 505
    • 271
    • 443
    • 104
    • 370
    • 322
    • 136
    • 373
    • 442
    • 524
    • 308
    • 354
    • 75
    • 279
    • 400
    • 196
    • 510
    • 110
    • 446
    • 78
    • 330
    • 73
    • 288
    • 285
    • 295
    • 406
    • 528
    • 329
    • 184
    • 350
    • 462
    • 304
    • 457
  • System Code722226
  • UDI00884838099272
  • System Serial Number

    861 of 861 codes

    • 120
    • 122
    • 123
    • 124
    • 125
    • 126
    • 127
    • 153
    • 67
    • 209
    • 271
    • 675
    • 112
    • 1052
    • 1091
    • 113
    • 121
    • 139
    • 158
    • 1078
    • 1145
    • 239
    • 105
    • 678
    • 114
    • 362
    • 758
    • 403
    • 702
    • 108
    • 545
    • 197
    • 380
    • 281
    • 688
    • 592
    • 593
    • 495
    • 319
    • 687
    • 921
    • 182
    • 183
    • 325
    • 690
    • 100
    • 272
    • 680
    • 724
    • 350
    • 891
    • 280
    • 270
    • 254
    • 107
    • 144
    • 761
    • 681
    • 691
    • 779
  • System Code722236
  • UDI00884838116788
  • System Serial Number

    243 of 243 codes

    • 127
    • 37
    • 159
    • 345
    • 24
    • 17
    • 25
    • 180
    • 150
    • 227
    • 235
    • 131
    • 288
    • 226
    • 231
    • 203
    • 26
    • 20
    • 249
    • 121
    • 200
    • 208
    • 42
    • 205
    • 36
    • 183
    • 81
    • 147
    • 148
    • 133
    • 31
    • 342
    • 54
    • 194
    • 43
    • 158
    • 99
    • 21
    • 40
    • 60
    • 118
    • 50
    • 378
    • 325
    • 335
    • 39
    • 191
    • 280
    • 233
    • 48
    • 197
    • 221
    • 68
    • 204
    • 51
    • 230
    • 38
    • 22
    • 186
    • 32
Amount recalled
1523 units (322 US, 1201 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, 5:37 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.