Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ingenia Ambition S (781359) Recalled by Philips Medical Systems Nederlands Due to Magnet Energization Device (MED) can have a residual...
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
Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED), Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device
Quantity: 4 units
Why Was This Recalled?
Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling.
Where Was This Sold?
This product was distributed to 1 state: FL
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