Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Medical System Allura Xper X-Ray Angiographic Recalled by Philips Medical Systems, Inc. Due to In certain circumstances, a software error can lead...
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 System Allura Xper X-Ray Angiographic
Quantity: 7439
Why Was This Recalled?
In certain circumstances, a software error can lead to a situation where the five minute fluoroscopy audible signal does not sound.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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