PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. 2026-04-08 Health serious FDA
Health · FDA · Recall #FDA-Z-1664-2026
ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; Recall
Issued April 8, 2026 · PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
In April 2026, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled the ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013;, 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
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
What you should do
- 1 Stop using ALLURA Xper FD20 Biplane; System Code: (1) 722008, (2)722013; 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.
Official remedy (Voluntary):
Recall details
- Brand
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Health
- Recall date
- April 8, 2026
- Units affected
- Not reported
- Sold at
- Domestic: Nationwide Distribution; International: Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, Bahamas, Bahrain,
- Recall number
- FDA-Z-1664-2026
- 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 356th Health recall we've logged in 2026.