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; pu…

Recall date

September 6, 2023

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2652-2023

FDA classification

Class II

Brand / firm

GE MEDICAL SYSTEMS, ISRAEL LTD.

Sold / distributed

Worldwide distribution - US Nationwide distribution including government and military distribution as well as PR.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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