GE Healthcare: Device Recall
Recall #Z-0039-2025 · 08/29/2024
Recall Details
- Recall Number
- Z-0039-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- GE Healthcare
- Status
- Ongoing
- Date Initiated
- 08/29/2024
- Location
- Chicago, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1500 units
Reason for Recall
GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) version v6.0 SP11.x where the latest report is not shown by default to the user. The issue may occur when a study has multiple DICOM structured reports (i.e. preliminary, final, and/or addendum) stored in different series.
Product Description
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model/Catalog/Code Numbers: a)¿¿¿¿¿ 2089507-120; b)¿¿¿¿ 2089507-129; c)¿¿¿¿¿ 2089507-131; d)¿¿¿¿ 2089507-135; e)¿¿¿¿ 2089507-136; f)¿¿¿¿¿¿ 2089507-140; g)¿¿¿¿¿ 2089507-144; h)¿¿¿¿ 2089507-145; i)¿¿¿¿¿¿ 2089507-149; j)¿¿¿¿¿¿ 2089507-153; k)¿¿¿¿¿ 2089507-154; l)¿¿¿¿¿¿ 2089507-155; m)¿¿¿ 2089507-156; n)¿¿¿¿ 2089507-157; o)¿¿¿¿ K2037DAED; p)¿¿¿¿ K2037DBED; q)¿¿¿¿ K2037DED; r)¿¿¿¿¿ K2037DJED; s)¿¿¿¿¿ K2037DNED; t)¿¿¿¿¿ K2042TTED; u)¿¿¿¿ K2049DC; v)¿¿¿¿¿ K2049DD; w)¿¿¿ K2049DF; x)¿¿¿¿¿ P2037DAED; y)¿¿¿¿¿ P2037DBED; z)¿¿¿¿¿ P2037DED; aa)¿¿ To be provided
Distribution Pattern
Worldwide distribution.
Other Recalls by GE Healthcare
- Class II: Risk 02/19/2025
- Class II: Risk 02/19/2025
- Class II: Risk 02/19/2025
- Class II: Risk 02/19/2025
- Class II: Risk 02/19/2025