---
title: "GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid... — FDA record Z-2316-2024 | Is It on Recall"
description: "GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and d"
url: https://isitonrecall.com/recall/fda-device-z-2316-2024-ge-vivid-ultrasound-products-model-numbers-a-vivid-e90-h45581lb-b-vivid-e95-h45581da/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA — FDA record Z-2316-2024

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 May 2, 2024. 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**: GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
- **Reason**: GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.
- **Classification**: Class II
- **Recalling firm**: GE Vingmed Ultrasound As
- **Quantity**: 7 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2316-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2316-2024%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 | a) H45581LB, UDI/DU \*, Serial Numbers: AU01170, AU01180, AU50159; b) H45581D, UDI/DI \*, Serial numbers: AU01095, AU50476, AU50252, AU01002 |

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

## Distribution

US: IL, MA, NM, NY, OK,

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

- [Illinois](https://isitonrecall.com/state/illinois/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [New Mexico](https://isitonrecall.com/state/new-mexico/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Oklahoma](https://isitonrecall.com/state/oklahoma/)

## Dates in the source

- **Report date**: Jul 17, 2024
- **Recall initiation date**: May 2, 2024
- **Center classification date**: Jul 5, 2024

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-2316-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [GE Vingmed Ultrasound As records](https://isitonrecall.com/brand/ge-vingmed-ultrasound-as/)