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

View all recalls by GE Healthcare →

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.