# FDA recall Z-2652-2023

> **GE MEDICAL SYSTEMS, ISRAEL LTD.** · Class II · device recall initiated 2023-09-06.

## 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

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-2652-2023
- **Recalling firm:** GE MEDICAL SYSTEMS, ISRAEL LTD.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-06
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** HAIFA, N/A, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2652-2023

## Citation

> AI Analytics. FDA recall Z-2652-2023. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2652-2023. Source: US FDA. Licensed CC0.

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