Reported Apr 8, 2026 · Ongoing

Azurion 7 B12; System Code: (1)722067, (2)722225, (3)722235;

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 B12
  • System Code
    • (1)722067
    • (2)722225
    • (3)722235
Lot codes and dates
  • (1)
  • System Code722067
  • UDI00884838085350
  • System Serial Number

    202 of 202 codes

    • 221
    • 42
    • 172
    • 173
    • 109
    • 250
    • 103
    • 192
    • 92
    • 114
    • 225
    • 69
    • 214
    • 41
    • 98
    • 81
    • 123
    • 278
    • 46
    • 277
    • 115
    • 150
    • 163
    • 131
    • 71
    • 104
    • 132
    • 147
    • 208
    • 244
    • 75
    • 36
    • 234
    • 141
    • 70
    • 26
    • 148
    • 133
    • 57
    • 128
    • 188
    • 151
    • 68
    • 233
    • 111
    • 255
    • 43
    • 33
    • 22
    • 146
    • 256
    • 270
    • 238
    • 187
    • 74
    • 154
    • 157
    • 251
    • 237
    • 222
  • System Code722225
  • UDI00884838099265
  • System Serial Number

    377 of 377 codes

    • 104
    • 153
    • 46
    • 28
    • 72
    • 208
    • 41
    • 122
    • 147
    • 376
    • 262
    • 331
    • 112
    • 110
    • 207
    • 375
    • 404
    • 405
    • 68
    • 177
    • 291
    • 299
    • 400
    • 29
    • 141
    • 216
    • 217
    • 71
    • 37
    • 175
    • 205
    • 228
    • 229
    • 157
    • 340
    • 453
    • 53
    • 259
    • 260
    • 300
    • 268
    • 55
    • 235
    • 298
    • 233
    • 354
    • 289
    • 148
    • 249
    • 434
    • 435
    • 409
    • 84
    • 111
    • 227
    • 455
    • 365
    • 284
    • 362
    • 468
  • System Code722235
  • UDI00884838116788
  • System Serial Number

    93 of 93 codes

    • 77
    • 127
    • 76
    • 88
    • 12
    • 43
    • 102
    • 59
    • 71
    • 11
    • 55
    • 57
    • 89
    • 13
    • 74
    • 105
    • 118
    • 125
    • 135
    • 41
    • 94
    • 70
    • 54
    • 72
    • 47
    • 4
    • 92
    • 139
    • 79
    • 93
    • 27
    • 78
    • 14
    • 20
    • 109
    • 108
    • 56
    • 106
    • 30
    • 31
    • 142
    • 107
    • 10
    • 3
    • 99
    • 137
    • 131
    • 82
    • 83
    • 84
    • 100
    • 126
    • 66
    • 67
    • 96
    • 63
    • 34
    • 28
    • 17
    • 18
Amount recalled
670 units (106 US, 564 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, 5:31 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.