FDASeptember 6, 2023device
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
Official recall recorded by the U.S. Food & Drug Administration.
The 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.
What to do
FDA enforcement status: Ongoing
Brands named
ge medical systems israel
UPCs
00840682138840084068219050300195278516510
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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