Use cautionMedical device recall · FDA · Published May 16, 2024
Philips Allura Xper FD10 System with ADN7NT Table Recall: Unintended Table Movement Risk
Philips recalls Allura Xper FD10 systems with ADN7NT patient tables (model 722010, software 8.1.100) due to risk of unintended table movement after software update. Affected units may require repair or replacement.
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Take action
Contact the company
📍Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Veenpluis 4-6 · Best, Netherlands
“Philips Allura Xper FD10 System with ADN7NT Table Recall: Unintended Table Movement Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/55054-philips-allura-xper-fd10-system-with-adn7nt-table-recall-unintended. Based on FDA recall #Z-1896-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1896-2024%22&limit=1).
The FDA announced on May 16, 2024, that Philips Medical Systems Nederland B.V. is recalling the Philips Allura Xper FD10 system with an ADN7NT patient table due to a software issue. The hazard involves unexpected table movements if Software upgrade 8.1.100 is installed.
How to tell if you have it
Brand: Philips
Product: Philips Allura Xper FD10 system with an ADN7NT patient table
Model Number: 722010
Software Version Number: 8.1.100
Product number: 722010
UDI/DI: 00884838059030
Serial Numbers: 774, 909, 526
The hazard
When Software upgrade 8.1.100 is installed on an Allura Xper with an AD7NT (non tilt) table, the pivot brake does not engage. This issue may cause unexpected movements of the table.
Context
GovInfoNow's records show PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 58 other recalls on record since 2021-05-26. Other recent recalls of similar products include IMRIS ORT300 Operating Room Table Recall (2026-08-06), IMRIS ORT200 Operating Room Table Recall (2026-08-06), and GE Optima XR200amx Mobile Radiography System Recall (2026-06-05).
How to tell if you have this one
Check for model number 722010 and software version 8.1.100 on the Philips Allura Xper FD10 system with an ADN7NT patient table. Serial numbers 774, 909, or 526 are also associated with this recall.
Brand
Philips
Category
Medical device
FDA recall event · 3 products
All 3 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
Domestic: OK International: India, Spain, U.A.E.
Recall number
Product, codes & lots
Quantity
Z-1895-2024
Philips Allura Xper FD20 system with an ADN7NT patient table. Model Number: 722012, Software Version Number 8.1.100.; Product number: 722012, UDI/DI: 00884838059054; Serial Number: 2138.
1 unit (US)
Z-1896-2024
Philips Allura Xper FD10 system with an ADN7NT patient table. Model Number: 722010, Software Version Number 8.1.100.; Product number: 722010, UDI/DI: 00884838059030; Serial Numbers: 774, 909, 526.
3 units (OUS)
Z-1897-2024
Philips Allura Xper FD20 Biplane system with an ADN7NT patient table. Model Number: 722013, Software Version Number 8.1.100.; Product number: 722013, UDI/DI: 00884838059061; Serial Number: 232.
1 unit (OUS)
Based on the official FDA remedy
What to do — step by step
Check Software Version
Verify the software version on your Philips Allura Xper FD10 system with ADN7NT table. If it is 8.1.100, it is affected.
Contact Philips Support
Reach out to Philips for guidance on whether your system needs repair or replacement.
Where it went and when
Where it was distributed
Distributed in Oklahoma, and outside the U.S.
Listed by the agency
Not listed
FDA distribution: “Domestic: OK International: India, Spain, U.A.E.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Oklahoma.
Recall timeline
FDA published this recall 20 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1896-2024 (May 16, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1896-2024 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.