Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ProxiDiagnost N90 Recalled by Philips North America, LLC Due to Unexpected increase in peak tube potential (kV) will...
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 North America, LLC directly.
Affected Products
ProxiDiagnost N90
Quantity: 71
Why Was This Recalled?
Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.
Where Was This Sold?
United States
About Philips North America, LLC
Philips North America, LLC has 88 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report