GE Vingmed Ultrasound As: Medical Device Recall in 2024 - (Recall #: Z-2316-2024)

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 E90, H45581LB; b) Vivid E95, H45581DA

Product Classification:

Class II

Date Initiated: May 2, 2024

Date Posted: July 17, 2024

Recall Number: Z-2316-2024

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: 7 units

Code Information:

a) H45581LB, UDI/DU *, Serial Numbers: AU01170, AU01180, AU50159; b) H45581D, UDI/DI *, Serial numbers: AU01095, AU50476, AU50252, AU01002

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated