Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Intera 1.0T Omni/Stellar Recalled by Philips Medical Systems Nederlands Due to There is a potential for the ceiling speaker(s)...
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 Nederlands directly.
Affected Products
Intera 1.0T Omni/Stellar, Model Number 781102. Nuclear Magnetic Resonance Imaging System
Quantity: 11226 total
Why Was This Recalled?
There is a potential for the ceiling speaker(s) to fall from their position and be pulled to the MR system by the magnetic field.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems Nederlands
Philips Medical Systems Nederlands has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report