Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Proteus XR/a (SlOK : K993090) Recalled by GE Healthcare, LLC Due to Intermittently not receiving an audible exposure indication upon...
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
Proteus XR/a (SlOK : K993090)
Quantity: 647 US; 167 OUS
Why Was This Recalled?
Intermittently not receiving an audible exposure indication upon completion of an exposure on the Proteus stationary radiographic system.
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