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FDA · Medical devices ·

Allura Xper FD recall

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled Allura Xper FD on August 19, 2026 because of firmware issue potentially leading to loss of geometry movements. It was sold nationwide.

Why it was recalled

Firmware issue potentially leading to loss of geometry movements.

What's recalled

Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.

Quantity: 4,252 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
Worldwide distribution - US Nationwide and the countries of Canada, Algeria, Argentina, Australia, Austria, Bangladesh, Belarus, Belgium, Brazil, Bulgaria, Chile, China, Colombia, Costa Rica, Croatia, Cuba, Czech Republic, Denmark, Ecuador, Egypt, Finland, France, French Polynesia, Germany, Greece,…
Status
Ongoing
Recall number
Z-2928-2026
Source
U.S. Food and Drug Administration

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