Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Venue Go Standard Carts Ref: (H45181VC and H45103VCW) Recalled by GE MEDICAL SYSTEMS, ISRAEL LTD. Due to Some Venue Go Standard Carts can develop 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 MEDICAL SYSTEMS, ISRAEL LTD. directly.
Affected Products
Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems; pulsed doppler imaging system
Quantity: 5986 devices
Why Was This Recalled?
Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE MEDICAL SYSTEMS, ISRAEL LTD.
GE MEDICAL SYSTEMS, ISRAEL LTD. 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