GE Healthcare: Device Recall
Recall #Z-3160-2024 · 07/23/2024
Class II: Risk
Recall Details
- Recall Number
- Z-3160-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- GE Healthcare
- Status
- Ongoing
- Date Initiated
- 07/23/2024
- Location
- Chicago, IL, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 803 units
Reason for Recall
Footprint Client (ZFP) versions v6.0 SP9.x and SP10.x where the latest addended report is not shown by default to the user. The issue occurs when the addendum is created on the same day as the original report but at a different time, and only when launched on the following browsers. " Internet Explorer 10 (IE10) " Internet Explorer 11 (IE11) " Firefox.
Product Description
GE Healthcare Centricity Universal Viewer Zero Footprint Client, Model Numbers: a) 2110344-008; b) 2110344-009; c) 2110344-010; d) 2110344-011; e) 2110344-013; f) 2110344-019; g) 2110344-025; h) 2110344-029; i) 2110344-030; j) 2110344-032 ; Radiological image processing system
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
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.