Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Table Patient Step on RFX/SFX Recalled by GE Healthcare, LLC Due to Reported incidents of a patient step detaching from...
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
Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
Quantity: 2,380 (2,215 US; 165 OUS)
Why Was This Recalled?
Reported incidents of a patient step detaching from the table. A fall from a patient step detaching while in use could result in an injury to a patient or operator.
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