Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips DigitalDiagnost Systems with M Cabinet Model: 712025 Stationary radiographic Recalled by Philips Healthcare Inc. Due to Creepage Distance between the two primary phases 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 Healthcare Inc. directly.
Affected Products
Philips DigitalDiagnost Systems with M Cabinet Model: 712025 Stationary radiographic system, digital-Universal RAD Applications
Quantity: 4 systems
Why Was This Recalled?
Creepage Distance between the two primary phases in the GEO Transformer is 4.5 mm.does not meet (IEC) International standard of 5.5 mm.
Where Was This Sold?
This product was distributed to 2 states: OH, WA
About Philips Healthcare Inc.
Philips Healthcare Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report