Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Healthcare Integris Allura 15 -12 Fluoroscopy x ray system Recalled by Philips Medical Systems, Inc. Due to Philips had discovered through a field service testing...
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 Healthcare Integris Allura 15 -12 Fluoroscopy x ray system
Quantity: one system
Why Was This Recalled?
Philips had discovered through a field service testing where a device failed to comply with a Federal standard.
Where Was This Sold?
This product was distributed to 1 state: FL
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