Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips DigitalDiagnost 3.1.x X-Ray System Recalled by Philips Electronics North America Corporation Due to During recent evaluations of the Philips DigitalDiagnost 3.1.x,...
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 Electronics North America Corporation directly.
Affected Products
Philips DigitalDiagnost 3.1.x X-Ray System
Quantity: US - 132
Why Was This Recalled?
During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Electronics North America Corporation
Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report