---
title: "Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2,... — FDA record Z-2652-2023 | Is It on Recall"
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 detach"
url: https://isitonrecall.com/recall/fda-device-z-2652-2023-venue-go-standard-carts-ref-h45181vc-and-h45103vcw-used-with-venue-go-r2-r3-r4-systems-r2-r3-and-r4/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems; ... — FDA record Z-2652-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Sep 6, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class II
- **Recalling firm**: GE MEDICAL SYSTEMS, ISRAEL LTD.
- **Quantity**: 5986 devices
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2652-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2652-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

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

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Ohio](https://isitonrecall.com/state/ohio/)
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- [Tennessee](https://isitonrecall.com/state/tennessee/)
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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Oct 11, 2023
- **Recall initiation date**: Sep 6, 2023
- **Center classification date**: Sep 29, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2652-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [GE MEDICAL SYSTEMS, ISRAEL LTD. records](https://isitonrecall.com/brand/ge-medical-systems-israel-ltd/)
