PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013.
Brand
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands
Lot Codes / Batch Numbers
Catalog numbers: (1) 722008, (2) 722013, UDI-DI: (1) No UDI, (2) 00884838059061, Serial Numbers: (1) 491, 489, 360, 325, 142, 312, 319, 516, 244, 453, 306, 378, 124, 18270, 524, 463, 197, 264, 294, 246, 320, 357, 212, 459, 472, 483, 465, 419, 38, 454, 441, 460, 369, 407, 231, 437, 105, 420, 1178, 270, 442, 521, 372, 254, 365, 390, 413, 379, 18, 239, 288, 424, 279, 481, 304, 267, 361, 415, 245, 445, 296, 487, 349, 456, 470, 386, 37, 205, 371, 416, 339, 513, 355, 337, 476, 121, 169, 327, 289, 518, 242, 93, 542, 122, 376, 543, 87, 391, 499, 253, 259, 393, 447, 495, 250, 110, 273, 31, 553, 433, 63, 398, 546, 213, 356, 408, 404, 448, 305, 475, 6001385, 425, 435, 450, 480, 370, 167, 323, 247, 525, 455, 394, 160, 350, 406, 274, 388, 283, 359, 8, 346, 335, 458, 410, 367, 266, 268, 482, 272, 385, 290, 468, 446, 46, 334 ****Serial Numbers Added 5/2/2025**** 378, 379, 516, 242, 274, 335, 367, 371, 393, (2) 505, 217, 313, 113, 34, 153, 410, 360, 290, 74, 83, 580, 160, 404, 126, 244, 106, 346, 383, 461, 307, 1, 442, 435, 293, 253, 297, 46, 289, 638, 342, 69, 267, 214, 402, 86, 603, 82, 149, 424, 140, 254, 255, 266, 475, 518, 519, 303, 194, 115, 150, 129, 496, 599, 441, 124, 151, 179, 550, 377, 575, 631, 562, 178, 330, 309, 601, 327, 73, 264, 78, 268, 308, 141, 175, 357, 85, 40, 216, 637, 422, 174, 109, 218, 228, 511, 389, 152, 479, 561, 262, 626, 61, 164, 497, 379, 84, 125, 241, 564, 573, 426, 556, 42, 100, 495, 500, 96, 515, 105, 428, 427, 531, 375, 316, 278, 347, 462, 249, 205, 246, 43, 639, 35, 480, 304, 634, 147, 15, 607, 52, 567, 283, 168, 171, 265, 509, 332, 272, 295, 97, 589, 444, 447, 292, 400, 628, 384, 206, 559, 538, 117, 629, 620, 624, 623, 215, 454, 416, 415, 47, 335, 222, 619, 598, 445, 361, 358, 549, 133, 476, 315, 36, 31, 390, 630, 17, 633, 417, 490, 48, 528, 53, 238, 525, 276, 560, 157, 247, 618, 372, 224, 76, 613, 478, 50, 544, 172, 232, 530, 349, 585, 608, 66, 296, 271, 359, 570, 457, 547, 183, 184, 185, 186, 187, 188, 189, 190, 413, 437, 107, 138, 225, 58, 29, 227, 318, 345, 139, 473, 388, 434, 64, 502, 586, 394, 275, 334, 411, 501, 450, 208, 408, 458, 258, 261, 429, 353, 395, 128, 348, 503, 557, 493, 563, 103, 396, 551, 250, 595, 406, 510, 355, 57, 535, 137, 569, 522, 436, 465, 201, 533, 135, 412, 95, 294, 344, 354, 425, 542, 207, 622, 182, 555, 524, 574, 366, 527, 324, 311, 459, 70, 161, 449, 321, 176, 65, 181, 554, 104, 167, 312, 130, 325, 470, 440, 144, 28, 385, 403, 448, 81, 380, 374, 256, 405, 60, 108, 468, 367, 455, 191, 301, 302, 352, 62, 300, 299, 71, 239, 506, 243, 378, 632, 110, 111, 158, 237, 453, 165, 364, 532, 223, 343, 291, 22, 370, 193, 163, 526, 236, 132, 156, 368, 177, 443, 259, 540 ****Serial Numbers Added 5/2/2025**** 35, 72, 73, 82, 113, 160, 480, 580, 76, 97, 272, 292, 396.
Products Sold
Catalog numbers: (1) 722008, (2) 722013; UDI-DI: (1) No UDI, (2) 00884838059061; Serial Numbers: (1) 491, 489, 360, 325, 142, 312, 319, 516, 244, 453, 306, 378, 124, 18270, 524, 463, 197, 264, 294, 246, 320, 357, 212, 459, 472, 483, 465, 419, 38, 454, 441, 460, 369, 407, 231, 437, 105, 420, 1178, 270, 442, 521, 372, 254, 365, 390, 413, 379, 18, 239, 288, 424, 279, 481, 304, 267, 361, 415, 245, 445, 296, 487, 349, 456, 470, 386, 37, 205, 371, 416, 339, 513, 355, 337, 476, 121, 169, 327, 289, 518, 242, 93, 542, 122, 376, 543, 87, 391, 499, 253, 259, 393, 447, 495, 250, 110, 273, 31, 553, 433, 63, 398, 546, 213, 356, 408, 404, 448, 305, 475, 6001385, 425, 435, 450, 480, 370, 167, 323, 247, 525, 455, 394, 160, 350, 406, 274, 388, 283, 359, 8, 346, 335, 458, 410, 367, 266, 268, 482, 272, 385, 290, 468, 446, 46, 334 ****Serial Numbers Added 5/2/2025**** 378, 379, 516, 242, 274, 335, 367, 371, 393; (2) 505, 217, 313, 113, 34, 153, 410, 360, 290, 74, 83, 580, 160, 404, 126, 244, 106, 346, 383, 461, 307, 1, 442, 435, 293, 253, 297, 46, 289, 638, 342, 69, 267, 214, 402, 86, 603, 82, 149, 424, 140, 254, 255, 266, 475, 518, 519, 303, 194, 115, 150, 129, 496, 599, 441, 124, 151, 179, 550, 377, 575, 631, 562, 178, 330, 309, 601, 327, 73, 264, 78, 268, 308, 141, 175, 357, 85, 40, 216, 637, 422, 174, 109, 218, 228, 511, 389, 152, 479, 561, 262, 626, 61, 164, 497, 379, 84, 125, 241, 564, 573, 426, 556, 42, 100, 495, 500, 96, 515, 105, 428, 427, 531, 375, 316, 278, 347, 462, 249, 205, 246, 43, 639, 35, 480, 304, 634, 147, 15, 607, 52, 567, 283, 168, 171, 265, 509, 332, 272, 295, 97, 589, 444, 447, 292, 400, 628, 384, 206, 559, 538, 117, 629, 620, 624, 623, 215, 454, 416, 415, 47, 335, 222, 619, 598, 445, 361, 358, 549, 133, 476, 315, 36, 31, 390, 630, 17, 633, 417, 490, 48, 528, 53, 238, 525, 276, 560, 157, 247, 618, 372, 224, 76, 613, 478, 50, 544, 172, 232, 530, 349, 585, 608, 66, 296, 271, 359, 570, 457, 547, 183, 184, 185, 186, 187, 188, 189, 190, 413, 437, 107, 138, 225, 58, 29, 227, 318, 345, 139, 473, 388, 434, 64, 502, 586, 394, 275, 334, 411, 501, 450, 208, 408, 458, 258, 261, 429, 353, 395, 128, 348, 503, 557, 493, 563, 103, 396, 551, 250, 595, 406, 510, 355, 57, 535, 137, 569, 522, 436, 465, 201, 533, 135, 412, 95, 294, 344, 354, 425, 542, 207, 622, 182, 555, 524, 574, 366, 527, 324, 311, 459, 70, 161, 449, 321, 176, 65, 181, 554, 104, 167, 312, 130, 325, 470, 440, 144, 28, 385, 403, 448, 81, 380, 374, 256, 405, 60, 108, 468, 367, 455, 191, 301, 302, 352, 62, 300, 299, 71, 239, 506, 243, 378, 632, 110, 111, 158, 237, 453, 165, 364, 532, 223, 343, 291, 22, 370, 193, 163, 526, 236, 132, 156, 368, 177, 443, 259, 540 ****Serial Numbers Added 5/2/2025**** 35, 72, 73, 82, 113, 160, 480, 580, 76, 97, 272, 292, 396.
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands is recalling Allura Xper FD20 Biplane; Catalog numbers: (1) 722008, (2) 722013. due to Possibility of the patient falling from the table related to the mattress used on the patient table.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possibility of the patient falling from the table related to the mattress used on the patient table.
Recommended Action
Per FDA guidance
On January 14, 2025 URGENT MEDICAL DEVICE CORRECTION letters were sent to customers. 4. Actions that should be taken by the customer / user in order to prevent risks for patients or users " Circulate this Urgent Medical Device Correction letter to all users of the system so that they are aware of the issue. " Follow the additional instructions on the use of the mattress included in Appendix B. These instructions include information for the transfer of the patient and the correct use and positioning of the mattress. The information of this Appendix is being included in an Addendum to the Instructions for Use. Additionally, Philips is creating a Quick Reference Card. The Addendum and the Quick Reference Card will be available as from end of March 2025. Please refer to Appendix C on how to download the Addendum to the Instructions for Use and the Quick Reference Card. " In case that the affected system has been transferred to another organization, please send a copy of this Urgent Medical Device Correction letter to that organization and inform Philips about this transfer through the email account: IGT_Recalls@philips.com " Please complete and return the Response form attached to Philips promptly and no later than 30 days from receipt. Completing this form confirms receipt of the Urgent Medical Device Correction letter and understanding of the issue and required actions to be taken. " Should you experience the issue reported in this letter, please report the event to Philips through your local Philips representative (1- 800-722-9377). 5. Actions planned by Philips Image Guided Therapy Systems to correct the problem Philips is informing customers of this issue through this Urgent Medical Device Correction. Additionally, Philips is releasing an Addendum to the Instructions for Use and a Quick Reference Card that will be available for customers at the end of March 2025. This Urgent Medical Device Correction letter has been reported to the appropriate Regulatory Agencies.
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This page aggregates publicly available data. Always confirm recall details directly with the U.S. Food and Drug Administration (FDA) before taking action.
View official FDA recall noticePage updated: Jan 10, 2026
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