Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers:… Recall
Issued October 1, 2025 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
In October 2025, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled the Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers:…, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
What you should do
- 1 Stop using Allura Xper FD20 Biplane Product Codes: (1)722013, (2) 722008; Associated 510(k) numbers:… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Recall details
- Brand
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Health
- Recall date
- October 1, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bangladesh, Belarus
- Recall number
- FDA-Z-2627-2025
- Made in
- Netherlands
- Issuing agency
- FDA
In context
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 17 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.