Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Medical Systems Allura Xper FD20C with software version R8.2.O Recalled by Philips Medical Systems, Inc. Due to Faulty Automatic Motion Controller (AMC), a problem in...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems, Inc. directly.
Affected Products
Philips Medical Systems Allura Xper FD20C with software version R8.2.O System Code: 722035. The Allura Xper FD series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and minimally invasive procedures.
Quantity: 2 units
Why Was This Recalled?
Faulty Automatic Motion Controller (AMC), a problem in the Power On Self Test (POST) error handling was detected, can result in a hazardous movement of the C-arc. system.
Where Was This Sold?
This product was distributed to 2 states: IL, TN
About Philips Medical Systems, Inc.
Philips Medical Systems, Inc. has 65 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report