Use caution Medical device recall · FDA · Published December 15, 2025

Philips Allura Xper FD10F Medical System Recall: Risk of Electrical Short-Circuits

Philips recalls Allura Xper FD10F medical systems with model 722002 due to potential coolant contact with electrical components causing short circuits and system shutdowns.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1063-2026Medical device Philips ›

Use caution until it’s fixed

Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.

Take action

Contact the company

Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Veenpluis 4-6 · Best, Netherlands

✎ GovInfoNow plain-language explainer

Philips is recalling all Allura Xper FD10F medical systems with model number 722002 because the drip tray under the cooling unit may not be properly installed. This could cause coolant to contact electrical parts, leading to short circuits and system shutdowns. Read more at govinfonow.com/recall/50430-philips-allura-xper-fd10f-medical-system-recall-risk-of-electrical.

Source Summary by GovInfoNow · govinfonow.com/recall/50430-philips-allura-xper-fd10f-medical-system-recall-risk-of-electrical · Updated August 17, 2026 · FDA enforcement record: FDA #Z-1063-2026

Cite this page

“Philips Allura Xper FD10F Medical System Recall: Risk of Electrical Short-Circuits.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/50430-philips-allura-xper-fd10f-medical-system-recall-risk-of-electrical. Based on FDA recall #Z-1063-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1063-2026%22&limit=1).

The FDA announced on Dec. 15, 2025, that Philips Medical Systems Nederland B.V. is recalling the Allura Xper FD10F medical device due to a potential coolant leak hazard. The agency issued recall number Z-1063-2026 for the Class II voluntary recall.

How to tell if you have it

Brand: Philips
Product Name: Allura Xper FD10F
Model Number: 722002
Serial Numbers: 61, 56, 27, 81, 25, 85, 20, 21, 84, 50, 31, 40

The hazard

The FDA stated that the drip tray beneath the cooling unit may not have been installed or adequately documented during previous field corrections. If missing, coolant liquid could contact electrical components, potentially causing short-circuits, fuse triggers, and system shutdowns.

Context

GovInfoNow's records show Philips Medical Systems Nederland B.V. has 58 other recalls on record since May 26, 2021. Other recent recalls of similar products include Philips IntelliVue MP70 Monitor Recall: No Alarms May Cause Health Risks (Oct. 31, 2025) and Philips Telemetry Monitor 5500 1.4 GHz Recall: Risk of Device Reset Causing Connection Failure (June 5, 2026). Recent brand recalls include software-related issues affecting Azurion R2.2.10 Systems reported on July 16, 2026, and a firmware issue potentially leading to loss of geometry movements reported on June 29, 2026.

How to tell if you have this one

Check for the model number 722002 on the Allura Xper FD10F system. This recall applies to systems that were not properly corrected or documented for the drip tray installation.

Brand
Philips
Category
Medical device

FDA recall event · 16 products

All 16 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Cayman Islands, Chile, China, Colombia, Costa Rica, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, France, Germany, Greece, Guatemala, Honduras, India, Italy, Japan, Kenya, Korea, Republic of, Malaysia, Mexico, Nepal, Netherlands, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Qatar, Romania, Russian Federation, Saudi Arabia, Singapore, South Africa, Spain, Sri Lanka, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Venezuela, Yemen.

Recall number	Product, codes & lots	Quantity
Z-1062-2026	Product Name: Allura Xper FD10C; Model number: 722001;; Model Number: 722001; System Product Name: Allura Xper FD10C; UDI-DI: N/A; Serial Numbers: 166, 181, 153, 274, 296, 267, 206, 247, 161, 282, 213, 284, 103, 199, 129, 95, 299, 30, 235, 221, 348, 283, 276, 253, 1100, 78, 229, 232, 159, 177, 219, 217, 205, 3, 89, 101, 295, 305;	38 units
Z-1063-2026	Allura Xper FD10F; Model Number: 722002;; Model Number: 722002; System Product Name: Allura Xper FD10F; UDI-DI: N/A; Serial Numbers: 61, 56, 27, 81, 25, 85, 20, 21, 84, 50, 31, 40;	12 units
Z-1064-2026	Allura Xper FD10; Model Number: 722003;; Model Number: 722003; System Product Name: Allura Xper FD10; UDI-DI: N/A; Serial Numbers: 1232, 967, 746, 1276, 232, 385, 1663, 1189, 81, 700, 167, 1072, 994, 150, 135, 1268, 168, 855, 213, 60, 471, 153, 319, 1159, 162, 180, 142, 1205, 719, 926, 426, 1413, 798, 65, 1165, 1658, 1193, 1778, 2933, 1585, 1380, 1706, 1613, 1685, 1297, 1388, 1522, 1238, 1416, 1448, 536, 1090, 1662, 1083, 1433, 1399, 62, 943, 249, 1227, 163, 1121, 1119, 889, 861, 1649, PP0200000118, 804, 1527, 468, 1593, 1198, 1022, 708, 1054, 865, 744, 1760, 936, 782, 953, 1035, 1058, 179, 1254, 1112, 389, 1560, 1660, 1013, 25, 215, 27;	93 units
Z-1065-2026	Allura Xper FD10/10; Model Number: 722005;; Model Number: 722005; System Product Name: Allura Xper FD10/10; UDI-DI: N/A; Serial Numbers: 93, 269, 530, 306, 307, 247, 53, 401, 141, 531, 184, 75, 276, 36;	14 units
Z-1066-2026	Allura Xper FD20; Model Number: 722006;; Model Number: 722006; System Product Name: Allura Xper FD20; UDI-DI: N/A; Serial Numbers: 1370, 1376, 225, 249, 1273, 1496, 707, 1466, 1141, 1201, 359, 105, 285, 1433, 822, 1747, 318, 797, 124, 1518, 384, 1045, 328, 302, 1536, 514, 910, 2123, 1360, 1381, 149, 379, 387, 1733, 197, 314, 888, 189, 310, 209, 863, 325, 378, 2110, 166, 118, 1978, 304, 1696, 2524, 248, 1928, 294, 804, 1227, 56, 245, 1560, 1795, 902, 1295, 1123, 1424, 1958, 40, 1222, 1947, 2289, 1687, 2304, 666, 2086, 958, 1801, 2546, 1317, 1478, 589, 2154, 1557, 1580, 519, 273, 157, 1504, 836, 1365, 393, 2428, 1902, 2433, 1521, 115, 2023, 1003, 1509, 1494, 2171, 2391, 867, 1513, 29, 951, 1814, 284, 482, 455, 1763, 1899, 1968, 837, 856, 1537, 93, 1561, 1746, 1232, 430, CV.797, 1974, 507, 1949, 1275, 1427, 1967, 374, 116, CV.507, 7567201, 2225, 267, 931, 344, 745, 233, 506, 2230, 1864, 457, 280, 1556, 640, 2;	143 units
Z-1067-2026	Allura Xper FD20 Biplane; Model Number: 722008;; Model Number: 722008; System Product Name: Allura Xper FD20 Biplane; UDI-DI: N/A; Serial Numbers: 296, 245, 141, 260, 13, 410, 196, 476, 488, 290, 339, 474, 383, 530, 722008530, 223, 468, 63;	18 units
Z-1068-2026	Allura Xper FD10; Model Number: 722010;; Model Number: 722010; System Product Name: Allura Xper FD10; UDI-DI: 00884838059030; Serial Numbers: 764, 1396, 728, 980, 782, 125, 1096, 661, 225, 1055, 1185, 368, 743, 1006, 570, 901, 552, 973, 795, 888, 1140, 781, 1060, 354, 186, 516, 517, 64, 386, 387, 530, 996, 964, 1265, 525, 307, 1189, 98, 774, 935, 721, 254, 1008, 1213, 1273, 66, 156, 304, 1422, 388, 235, 236, 1066, 1090, 549, 689;	56 units
Z-1069-2026	Allura Xper FD10/10; Model Number: 722011;; Model Number: 722011; System Product Name: Allura Xper FD10/10; UDI-DI: 00884838059047; Serial Numbers: 268, 205, 213, 89, 293, 294, 116, 272, 113, 152, 112, 139, 141, 111, 81, 66, 46, 153, 115, 114, 274;	21 units
Z-1070-2026	Allura Xper FD20; Model Number: 722012;; Model Number: 722012; System Product Name: Allura Xper FD20; UDI-DI: 00884838059054; Serial Numbers: 2942, 1515, 1189, 1594, 535, 1964, 2156, 2742, 2092, 1673, 1803, 1655, 2020, 1973, 2037, 1853, 2098, 1248, 1082, 1576, 1057, 1129, 646, 930, 1421, 462, 203, 627, 2005, 1428, 353, 288, 191, 1994, 1802, 156, 853, 1283, 1956, 2361, 1980, 872, 931, 1295, 2513, 1090, 1374, 468, 1822, 812, 1379, 1817, 1580, 1050, 309, 144, 1841, 1845, 1468, 558, 1968, 1959, 2168, 1168, 1562, 967, 2114, 47, 167, 2091, 2053, 604, 603, 217, 2918, 373, 850, 1820, 1821, 1619;	79 units
Z-1071-2026	Allura Xper FD20 Biplane; Model Number: 722013;; Model Number: 722013; System Product Name: Allura Xper FD20 Biplane; UDI-DI: 00884838059061; Serial Numbers: 601, 230, 370, 27, 320, 193, 60, 373, 560, 400, 549, 506, 381, 382, 132, 169, 233, 236, 243, 526, 447, 163, 403;	23 units
Z-1072-2026	Allura Xper FD20 OR Table; Model Number: 722023;; Model Number: 722023; System Product Name: Allura Xper FD20 OR Table; UDI-DI: 00884838059085; Serial Numbers: 103, 10, 85, 125;	4 units
Z-1073-2026	Allura Xper FD10; Model Number: 722026;; Model Number: 722026; System Product Name: Allura Xper FD10; UDI-DI: 00884838054189; Serial Numbers: 969, 223, 648, 664, 622, 931, 128, 616, 497, 769, 143, 881, 809, 18, 326, 794, 174, 804, 424, 587, 172, 911, 294, 569, 141, 161, 182, 928, 960, 858, 494, 628, 749, 968, 17, 273, 43, 203, 546, 104, 430, 575, 180, 594, 359, 723, 779, 632, 183, 330, 726, 637, 300, 429, 810, 995, 293, 296, 573, 917, 695, 676, 913, 274, 734, 520, 27, 940, 597, 598, 301, 818, 916, 328, 912, 691, 410, 873, 868, 816, 732, 147, 742, 651, 919, 89, 918, 346, 250, 755, 199, 255, 524, 256, 623;	95 units
Z-1074-2026	Allura Xper FD10/10; Model Number: 722027;; Model Number: 722027; System Product Name: Allura Xper FD10/10; UDI-DI: 00884838054196; Serial Numbers: 298, 246, 146, 170, 238, 162, 7, 99, 81, 126, 55, 86, 6, 259, 205, 60, 57, 63, 145, 182, 48, 278;	22 units
Z-1075-2026	Allura Xper FD20; Model Number: 722028;; Model Number: 722028; System Product Name: Allura Xper FD20; UDI-DI: 00884838054202; Serial Numbers: 893, 614;	2 units
Z-1076-2026	Allura Xper FD20/10; Model Number: 722029;; Model Number: 722029; System Product Name: Allura Xper FD20/10; UDI-DI: 00884838054219; Serial Numbers: 30, 81, 80, 47;	4 units
Z-1077-2026	Allura Xper FD20/20; Model Number: 722038;; Model Number: 722038; System Product Name: Allura Xper FD20/20; UDI-DI: 00884838054226; Serial Numbers: 11, 117, 110, 134, 64, 90, 124, 72;	8 units

Based on the official FDA remedy

What to do — step by step

Check Drip Tray Installation
Verify that the drip tray beneath the cooling unit is properly installed and documented as per field corrections.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Bangladesh, Belgium, Brazil, Cayman Islands, Chile, China, Colombia, Costa Rica, Cuba, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, France,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 37 days after the firm started it.

Dec 15, 2025Firm started the recall
Jan 13, 2026FDA classified it Class II
Jan 21, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/50430-philips-allura-xper-fd10f-medical-system-recall-risk-of-electrical">Philips Allura Xper FD10F Medical System Recall: Risk of Electrical Short-Circuits (GovInfoNow)</a>

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1063-2026 (December 15, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1063-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.