GE MEDICAL SYSTEMS, ISRAEL LTD.: Medical Device Recall in 2023 - (Recall #: Z-2652-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 6, 2023

Date Posted: October 11, 2023

Recall Number: Z-2652-2023

Event ID: 93069

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 5986 devices

Code Information:

Venue Go Standard Carts, Ref: (H45181VC and H45103VCW) used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems (GTIN 0084068213884, 00840682190503, and 00195278516510) that were manufactured 2022-08 and before

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated