Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE NM/CT 850 system Model Number H3907AD - Product Usage: Recalled by GE Healthcare, LLC Due to GE Healthcare has become aware that rotor bearing...
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
GE NM/CT 850 system Model Number H3907AD - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.
Quantity: 24 units
Why Was This Recalled?
GE Healthcare has become aware that rotor bearing screws were found loose on one detector in the field, leading to the release of one of the four rotor bearings in the detector.
Where Was This Sold?
Worldwide
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