Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Precision MPi is an all-digital multipurpose tilt-C x-ray system Recalled by Regulatory Insight, Inc Due to It was discovered that the Remote Touch Panel...
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 Regulatory Insight, Inc directly.
Affected Products
GE Precision MPi is an all-digital multipurpose tilt-C x-ray system, intended for a multitude of diagnostic procedures, including radiology, fluoroscopy, interventional procedures, vascular and non-vascular procedures, and specialized applications including angiographic studies.
Quantity: 43
Why Was This Recalled?
It was discovered that the Remote Touch Panel (RTP) of the GE Precision MPi X-ray system may not always boot up as intended and needs to be updated to properly accomplish its intended purpose.
Where Was This Sold?
This product was distributed to 17 states: CA, CO, FL, IN, MA, MI, MN, MS, NV, NY, OH, OR, PA, TN, VT, WA, WI
About Regulatory Insight, Inc
Regulatory Insight, Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report