GE Vingmed Ultrasound As: Medical Device Recall in 2024 - (Recall #: Z-2317-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW

Product Classification:

Class II

Date Initiated: May 2, 2024

Date Posted: July 17, 2024

Recall Number: Z-2317-2024

Event ID: 94772

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 1 unit

Code Information:

a) H45041SW, UDI/DI *, Serial Numbers: 001423S70

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated