GE Healthcare: Medical Device Recall in 2023 - (Recall #: Z-0143-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Universal Viewer Workflow Manager, Image processing radiological system

Product Classification:

Class II

Date Initiated: September 8, 2023

Date Posted: November 1, 2023

Recall Number: Z-0143-2024

Event ID: 93053

Reason for Recall:

When using Universal Viewer or Centricity Universal Viewer with Workflow Manager (WFM), if a third-party reporting application is used to launch exams, it could display information on a different patient than WFM and the Viewer.

Status: Ongoing

Product Quantity: 57 units

Code Information:

UDI/DI 00195278379610, Software versions 7.0 SP1.1, 7.0 SP1, 7.0 SP0.0.5, 7.0 SP0.1.0. All product IDs with an affected software version are impacted.

Distribution Pattern:

Nationwide distribution to AR, AZ, CA, CO, DE, FL, GA, IL, IN, ME, MI, MN, MO, NE, NJ, NM, NV, NY, OH, OK, PA, SC, SD, TN, TX. International distribution to Austria, Canada, France, Germany, Hong Kong, Israel, Italy, Philippines, Singapore, Thailand, Turkey, Vietnam.

Voluntary or Mandated:

Voluntary: Firm initiated