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GE MEDICAL SYSTEMS, ISRAEL LTD. recalls Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems; pul
Recalled October 11, 2023 · FDA recall Z-2652-2023 · GE MEDICAL SYSTEMS, ISRAEL
Hazard
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. · FDA Class II
Units
5986 devices
Sold at
Worldwide distribution - US Nationwide distribution including government and military distribution as well as PR.
Description
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.
Product
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
Manufacturer(s)
GE MEDICAL SYSTEMS, ISRAEL LTD.
Made in
Israel
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →