Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SIGNA Creator Recalled by GE Healthcare, LLC Due to GE Healthcare has recently become aware of an...
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
SIGNA Creator, SIGNA Explorer, Nuclear Magnetic Resonance Imaging System
Quantity: 1737 devices
Why Was This Recalled?
GE Healthcare has recently become aware of an issue on the affected products listed below where the "Patient Orientation" button may inadvertently be clicked when intending to click on the "Save RX" button. This changes the prescribed patient orientation on the system prior to running the initial 3-Plane Localizer Scan (See Figure 1 for reference to buttons.) Selecting and saving a patient orientation that does not match the patient's actual position may result in incorrectly annotated and/or flipped images.
Where Was This Sold?
Worldwide distributions.
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