Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AdvantageSim MD versions 7.4 through 7.6 Recalled by GE Healthcare, LLC Due to It was reported by a customer site that...
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
AdvantageSim MD versions 7.4 through 7.6, Model 5160092-2 Version 7.4, 5160092-3 Version 7.5, 5160092-4 version 7.6.
Quantity: 65
Why Was This Recalled?
It was reported by a customer site that when using GE AdvantageSim MD on Advantage Workstation, the series could be incorrectly labeled in image view when multiple series of an exam are loaded simultaneously in Advantage Sim MD and if their series dates are different. A mismatch of series label for structure sets may lead to under-treatment of a tumor due to too small coverage of volume treated.
Where Was This Sold?
This product was distributed to 13 states: AL, CT, FL, IL, MA, MO, NJ, NY, PA, TX, VA, WA, WI
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