Device recalls

Allura Xper FD20/15; Catalog numbers: 722058

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Possibility of the patient falling from the table related to the mattress used on the patient table.

Open, ClassifiedUnder Investigation by firmZ-1149-2025
Open FDA's page for this record
Cfres ID
212097
Product res number
Z-1149-2025
Event date initiated
2025-01-13
Event date posted
2025-02-20
Recall status
Open, Classified
Res event number
96132
Product code
OWB
Product description
Allura Xper FD20/15; Catalog numbers: 722058
Firm FEI number
3002807880
Recalling firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Address 1
Veenpluis 4-6 4-6 veenpluis
City
Best
Country
Netherlands
Reason for recall
Possibility of the patient falling from the table related to the mattress used on the patient table.
Root cause description
Under Investigation by firm
Product quantity
302 units (69 US, 233 OUS)
Code info

Catalog number: 722058; UDI-DI: 00884838059115; Serial Numbers: 172, 337, 178, 249, 22, 202, 279, 254, 285, 71, 186, 82, 85, 162, 138, 24, 365, 203, 167, 146, 168, 304, 200, 123, 129, 149, 259, 4, 197, 134, 38, 290, 171, 56, 264, 238, 199, 61, 156, 99, 65, 59, 109, 100, 305, 319, 215, 278, 124, 196, 405, 325, 265, 378, 277, 274, 94, 182, 340, 366, 190, 219, 373, 239, 23, 205, 257, 212, 111, 110, 35, 108, 32, 161, 6, 49, 89, 18, 19, 336, 392, 416, 398, 399, 412, 379, 333, 418, 385, 331, 413, 419, 400, 421, 395, 394, 408, 380, 409, 393, 369, 360, 389, 356, 357, 382, 415, 358, 411, 387, 335, 381, 370, 422, 407, 423, 397, 367, 396, 404, 420, 66, 163, 211, 214, 55, 40, 133, 114, 72, 96, 15, 9, 39, 150, 25, 81, 84, 119, 177, 268, 3, 60, 131, 377, 164, 7, 206, 101, 246, 384, 220, 261, 244, 348, 233, 106, 229, 223, 145, 136, 137, 288, 76, 86, 179, 112, 351, 130, 166, 276, 237, 45, 210, 181, 33, 251, 144, 64, 79, 29, 113, 21, 102, 36, 266, 295, 245, 243, 16, 41, 242, 187, 10, 345, 218, 361, 90, 193, 70, 26, 194, 53, 153, 234, 34, 235, 247, 272, 195, 87, 43, 31, 221, 75, 20, 330, 208, 189, 303, 63, 37, 117, 73, 230, 116, 148, 284, 236, 98, 95, 240, 350, 169, 376, 313, 343, 241, 192, 185, 115, 375, 154, 327, 92, 334, 232, 151, 201, 269, 332, 292, 142, 256, 391, 128, 344, 226, 141, 78, 183, 125, 126, 320, 248, 77, 368, 315, 68, 139, 311, 67, 347, 222, 93, 213, 354, 355, 58, 143, 301, 170, 159, 30, 103, 88, 386, 349, 252, 388, 11, 372, 281, 204, 127, 258, 289, 291, 293, 27, 97, 48, 188, 273.

Action

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.

Distribution pattern

Worldiwde distribution - US Nationwide and the countries of Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Bosnia and Herzegovina, Brazil, Brunei Darussalam, Bulgaria, Cambodia, Cayman Islands, Chile, China, Colombia, Costa Rica, C¿te D'Ivoire, Croatia, Cuba, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Ethiopia, Fiji, Finland, France, French Polynesia, Georgia, Germany, Ghana, Gibraltar, Greece, Guadeloupe, Guatemala, Guinea, Honduras, Hong Kong, Hungary, Iceland, India, Indonesia, Iran, Iraq, Ireland, Israel, Italy, JAMAICA, Japan, Jordan, Kazakhstan, Kenya, Korea, Republic of, Kosovo, Kuwait, Kyrgyzstan, Lao People's Democratic Republic, Latvia, Lebanon, Libya, Lithuania, Macao, Macedonia, Malaysia, Maldives, Malta, Martinique, Mauritania, Mauritius, Mexico, Moldova, Mongolia, Morocco, Myanmar, Nepal, Netherlands, New Caledonia, New Zealand, Nicaragua, Nigeria, Norway, Oman, Pakistan, Palestine, State of, Panama, Papua New Guinea, Paraguay, Peru, Philippines, Poland, Portugal, Qatar, R¿union, Romania, Russian Federation, Saudi Arabia, Senegal, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sri Lanka, Sudan, Sweden, Switzerland, Syrian Arab Republic, Taiwan, Tanzania, Thailand, Trinidad and Tobago, Tunisia, Turkey, Turkmenistan, Ukraine, United Arab Emirates, United Kingdom, Uruguay, Uzbekistan, Venezuela, Viet Nam, Yemen.

K numbers
K130842, K162859, K033737
Harmonized identifiers (openFDA)
Device name
Interventional Fluoroscopic X-Ray System
Medical specialty description
Radiology
Regulation number
892.1650
Device class
2
K number
K022322, K122457, K190768, K221344, K213455, K261413, K221335, K201156, K023178, K052412, K172863, K936180, K130893, K143225, K113027, K123508, K142243, K142273, K062647, K181830, K250010, K121444, K210054, K230950, K170144, K242731, K172700, K211191, K040675, K193326, K252500, K170800, K230185, K113403, K082243, K173664, K132094, K123529, K073543, K210900 +285 more
Registration number
3018094310, 3012624817, 3005172103, 3015223550, 3002672225, 3006972752, 3010703925, 3003768277, 3005706667, 3021559833, 3017375271, 3012957335, 3010398867, 2247992, 1054713, 3030412764, 3003477135, 3008284470, 3009196578, 3021060474, 3031503890, 3001722928, 3006544299, 3011015597, 3010462278, 3042175844, 3026391023, 3004977335, 3005843418, 3025394757, 3018596740, 3014343100, 3010162973, 1056553, 2031966, 3013184485, 3002466018, 3010685285, 1720753, 3027339477 +86 more
FEI number
3018094310, 3012624817, 3005172103, 3015223550, 3002672225, 3006972752, 3010703925, 3005706667, 3021559833, 3017375271, 3012957335, 3010398867, 3002808382, 3030412764, 3003477135, 3008284470, 3009196578, 3021060474, 3031503890, 3000209794, 3001722928, 3006544299, 3011015597, 3010462278, 3042175844, 3026391023, 3004977335, 3002619595, 3002175190, 3005843418, 3025394757, 3018596740, 3014343100, 3013184485, 3002466018, 3010685285, 1720753, 3000205591, 1000517638, 3027339477 +86 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.