Use caution Medical device recall · FDA · Published November 24, 2021

Philips Allura Xper X-ray System Recall: Cooling Leak Risk

Philips recalls specific Allura Xper X-ray systems with a leaky cooling system that could drip onto electrical parts, causing fire or smoke. Affected models include 722003-722039.

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

🇺🇸 FDA recall #Z-0724-2022Medical device Philips ›

Use caution until it’s fixed

Due to a leak in the detector cooling system, cooling liquid may leak outside the drip tray of the chiller. If this occurs the liquid may drip onto electrical components in the R cabinet located in the technical room, which could lead to damage to the system and potentially cause thermal events such as a burning odor, smoke or fire.

Take action

Contact the company

Recalling firmPhilips North America Llc222 Jacobs St · Cambridge, MA 02141-2289

✎ GovInfoNow plain-language explainer

Philips is recalling certain Allura Xper X-ray systems due to a leak in the cooling system that could drip onto electrical components, potentially causing smoke, fire, or system damage. This risk applies to specific model numbers and serial numbers listed in the recall. Read more at govinfonow.com/recall/61500-philips-allura-xper-x-ray-system-recall-cooling-leak-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/61500-philips-allura-xper-x-ray-system-recall-cooling-leak-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0724-2022

Cite this page

“Philips Allura Xper X-ray System Recall: Cooling Leak Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61500-philips-allura-xper-x-ray-system-recall-cooling-leak-risk. Based on FDA recall #Z-0724-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0724-2022%22&limit=1).

The FDA announced on 2021-11-24 that Philips North America Llc is recalling Philips Allura Xper and UNIQ interventional fluoroscopic X-ray systems with a Laird chiller due to potential thermal events. The hazard involves cooling liquid leaking onto electrical components, which could cause smoke or fire. This Class II recall affects 63 systems in the USA and 127 abroad.

How to tell if you have it

Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray
Model Numbers: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025, 722026, 722027, 722029, 722033, 722034, 722036, 722038, 722039
UPCs: 00884838054189, 00884838054202, 00884838054219

The hazard

Context

GovInfoNow's records show Philips North America Llc has 129 other recalls on record since 2017-07-12. Recent brand recalls include a 2026-08-21 recall of SmartPath to dStream systems for a software issue terminating examinations and a 2026-08-18 recall of Spectral CT 7500 Scanners for potential extra radiation exposure. Other recent recalls of similar products include Philips Allura Xper FD20/10: Coolant Risk in Drip Tray Not Installed (2025-12-15), Philips Allura Xper FD20 Biplane Recall: Coolant Risk if Drip Tray Not Installed (2025-12-15), and Philips Allura Xper FD20: Coolant Risk If Drip Tray Not Installed (2025-12-15).

How to tell if you have this one

Check for model numbers 722003 through 722039 or serial numbers listed in the recall notice. The affected units lack an extended drip tray for the chiller.

Brand
Philips
Product
Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird
Category
Medical device

FDA recall event · 2 products

All 2 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
US Nationwide Foreign: Argentina Austria Bangladesh Brazil Chile China Denmark Dominican Republic France Germany Greece India Indonesia Iran Israel Italy Japan Korea, Republic of Malaysia Mexico Netherlands Philippines Russian Federation Saudi Arabia South Africa Spain Sri Lanka Switzerland Taiwan Thailand Turkey United Kingdom Virgin Islands (U.S.)

Recall number	Product, codes & lots	Quantity
Z-0724-2022	Philips Allura Xper, UNIQ(Allura Xper system-China) Interventional Fluoroscopic X-ray System products with a Laird chiller WITHOUT an extended drip tray: Model Number: 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722014, 722015, 722019, 722020, 722022, 722023, 722024, 722025, 722026, 722027, 722029, 722033, 722034, 722036, 722038, 722039. Allura Xper F010 {C+F). 722003 Allura Xper F010/10 722005 Allura Xper F020 722006 Allura Xper F020/10 and F020/20 722008 Allura Xper F010 722010 Altura Xper F010/10 722011 Allura Xper F020 722012 Allura Xper FD20 biplane 722013 Allura Xper FDlO OR Table 722014 Allura Xper FD20 OR Table 722015 Allura Xper FDl0/10 OR Table 722019 Allura Xper FD20 Biplane OR Table 722020 Allura Xper FD10 OR Table 722022 Allura Xper FD20 OR Table 722023 Allura Xper FD10/10 OR Table 722024 Altura Xper FD20 Biplane OR Table 722025 Allura Xper FD10 722026 Allura Xper FD10/10 722027 Altura Xper FD20/10 biplane 722029 Allura Xper FD10 OR Table 722033 Allura Xper FD10/10 OR Table 722034 Allura Xper FD20/10 OR Table 722036 Allure Xper F020/20 722038 Altura Xper FD20/20 biplane OR Table 722039; Allura Xper FD10 722003/722026 (US) S/N: 24 40 71 162 191 266 283 294 319 347 406 485 825 959 965 967 985 990 1246 1353 1444 1944 1949 UDI: (01)00884838054189(21)825 (01)00884838054189(21)967 (01)00884838054189(21)1246 (01)00884838054189(21)965 (01)00884838054189(21)959 (01)00884838054189(21)990 (01)00884838054189(21)985 Allura Xper FD10/10 722005 S/N: 144 US OUS: 37 52 74 79 80 108 279 417 459 Allura Xper FD20 722006 S/N: US 44 72 234 246 263 268 327 333 429 469 471 498 514 535 550 554 588 604 718 754 766 861 1174 1274 1355 1400 1783 1831 1844 1878 1886 1931 2018 UDI: (01)00884838054202(21)893 OUS: 11 40 89 102 112 125 151 244 364 408 431 484 568 580 594 597 602 640 643 704 811 940 971 1262 1312 1402 1405 1424 1465 1481 1658 1691 1794 1796 1815 1852 1859 1879 1891 1948 1959 1974 1985 1988 2141 2311 2521 2554 Allura Xper FD20 Biplane 722008 S/N: 33, 82, 374 (US) OUS: 39 86 224 249 336 384 388 532 Allura Xper FD10 722010 S/N:OUS 163 340 1422 1429 1434 Allura Xper FD20 722012 S/N: OUS 395 463 927 1013 1518 2652 2854 2918 Allura Xper FD20 OR Table 722015 S/N: 30 (OUS) Allura Xper FD10 722026 S/N OUS: 315 701 748 884 888 943 948 960 971 975 978 984 989 995 Allura Xper FD10/10 722027 S/N: OUS 268 278 Allura Xper FD20/10 722029 S/N:OUS 9 Allura Xper FD10 722026 S/N : US 825 959 965 967 985 990 1246 OUS: 11 40 89 102 112 125 151 244 364 408 431 484 568 580 594 597 602 640 643 704 811 940 971 1262 1312 1402 1405 1424 1465 1481 1658 1691 1794 1796 1815 1852 1859 1879 1891 1948 1959 1974 1985 1988 2141 2311 2521 2554 Allura Xper FD10/10 266 722027 S/N: 266 Allura Xper FD20 722028 S/N: 893 UDI: (01)00884838054202(21)893 Allura Xper FD20/10 722029 S/N: 91, 94 US UDI: (01)00884838054219(21)94 OUS: S/N:6	USA: 63 systems R.O.W.: 127 systems
Z-0725-2022	Philips Allura CV20 Interventional Fluoroscopic X-ray System products with a Laird chiller without an extended drip tray: Model Number: 722031; S/N: OUS 109	1 unit

Based on the official FDA remedy

What to do — step by step

Check Model and Serial Numbers
Compare your unit's model number and serial number against the list provided in the recall notice to confirm if it is affected.
Contact Philips for Guidance
Reach out to Philips directly for specific instructions on whether your unit needs repair or replacement.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “US Nationwide Foreign: Argentina Austria Bangladesh Brazil Chile China Denmark Dominican Republic France Germany Greece India Indonesia Iran Israel Italy Japan Korea, Republic of Malaysia Mexico Netherlands Philippines Russian Federation…” 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 4 months after the firm started it.

Nov 24, 2021Firm started the recall
Mar 4, 2022FDA classified it Class II
Mar 16, 2022Published 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/61500-philips-allura-xper-x-ray-system-recall-cooling-leak-risk">Philips Allura Xper X-ray System Recall: Cooling Leak Risk (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-0724-2022 (November 24, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0724-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.