Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: Recalled by Philips Medical Systems Nederlands Due to Certain low-voltage DC power supplies (DCPS) used 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 Nederlands directly.
Affected Products
Philips Allura Xper System: Interventional Fluoroscopic X-Ray System Product No.: 722026, 722027, 722028, 722029, 722035, 722038, and 722058.
Quantity: 42 devices
Why Was This Recalled?
Certain low-voltage DC power supplies (DCPS) used in these products may be subject to an increased probability of failure. Failure of a DCPS may result in the sudden loss of imaging functionality or mechanical movement, depending on what subsystems the DCPS is powering.
Where Was This Sold?
This product was distributed to 10 states: AL, AZ, FL, GA, IL, MA, MO, NJ, OR, VA
About Philips Medical Systems Nederlands
Philips Medical Systems Nederlands has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report