Reported Apr 8, 2026 · Ongoing

Azurion 7 M12; System Code: (1)722078, (2)722223, (3)722233;

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 M12
  • System Code
    • (1)722078
    • (2)722223
    • (3)722233
Lot codes and dates
  • (1)
  • System Code722078
  • UDI00884838085251
  • System Serial Number

    779 of 779 codes

    • 302
    • 585
    • 410
    • 753
    • 523
    • 293
    • 840
    • 291
    • 536
    • 537
    • 870
    • 613
    • 598
    • 679
    • 224
    • 829
    • 249
    • 546
    • 478
    • 479
    • 513
    • 278
    • 437
    • 438
    • 456
    • 566
    • 833
    • 488
    • 327
    • 550
    • 571
    • 544
    • 545
    • 465
    • 376
    • 31
    • 921
    • 700
    • 165
    • 445
    • 539
    • 654
    • 656
    • 657
    • 658
    • 436
    • 1007
    • 862
    • 786
    • 308
    • 396
    • 576
    • 121
    • 239
    • 383
    • 491
    • 125
    • 500
    • 645
    • 379
  • System Code722223
  • UDI00884838099241
  • System Serial Number

    1,034 of 1,034 codes

    • 312
    • 324
    • 332
    • 585
    • 85
    • 533
    • 189
    • 479
    • 1038
    • 47
    • 1146
    • 352
    • 391
    • 328
    • 681
    • 1052
    • 1130
    • 388
    • 581
    • 855
    • 905
    • 570
    • 77
    • 448
    • 495
    • 571
    • 171
    • 1051
    • 439
    • 126
    • 628
    • 36
    • 1088
    • 580
    • 1179
    • 1241
    • 1065
    • 799
    • 577
    • 1060
    • 1107
    • 1114
    • 323
    • 252
    • 626
    • 261
    • 207
    • 329
    • 1001
    • 801
    • 560
    • 561
    • 205
    • 379
    • 440
    • 204
    • 192
    • 197
    • 177
    • 37
  • System Code722233
  • UDI00884838116764
  • System Serial Number

    183 of 183 codes

    • 64
    • 122
    • 169
    • 170
    • 267
    • 96
    • 144
    • 212
    • 153
    • 259
    • 118
    • 214
    • 41
    • 59
    • 124
    • 147
    • 103
    • 108
    • 111
    • 172
    • 127
    • 192
    • 218
    • 219
    • 250
    • 123
    • 37
    • 38
    • 183
    • 273
    • 304
    • 17
    • 137
    • 76
    • 300
    • 12
    • 201
    • 238
    • 82
    • 288
    • 295
    • 297
    • 298
    • 8
    • 141
    • 26
    • 27
    • 235
    • 68
    • 14
    • 138
    • 139
    • 117
    • 279
    • 58
    • 240
    • 28
    • 7
    • 280
    • 281
Amount recalled
1994 units (360 US, 1634 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, 5:40 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.