Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Various GE Magnetic Resonance System on-site software version Product Usage: Recalled by GE Healthcare, LLC Due to Possible incorrect software version loaded.
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 GE Healthcare, LLC directly.
Affected Products
Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for general diagnostic use
Quantity: 3,849
Why Was This Recalled?
Possible incorrect software version loaded.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Healthcare, LLC
GE Healthcare, LLC has 474 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report