GE Healthcare Recalls Centricity Universal Viewer Zero Footprint Client Due to Patient Data Mismatch
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
GE Healthcare has initiated a voluntary recall of 250 units of its radiological image processing software due to a defect where displayed patient information may not match the images shown.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 2, 2026 and geographically references Worldwide. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
GE Healthcare has initiated a voluntary recall of the Centricity Universal Viewer Zero Footprint Client (ZFP). The recall was prompted by a software defect where, under certain workflows, patient information shown in the viewer may not match the images actually displayed. This issue occurs on systems with Patient Timeline installed using specific software versions.
Which Products Are Affected
The recall affects 250 units of the GE Healthcare Centricity Universal Viewer Zero Footprint Client, classified as a radiological image processing system. The affected software versions are ZFP v6.0: SP11.6, SP11.6.0.1, and SP11.6.1.
Specific model numbers and UDI information include:
- Model Numbers: 2110344-039, 2110344-046, 2110344-047
- UDI/DI: 00840682102988
- Recall Number: Z-1475-2026
The distribution of these units is worldwide, including the United States nationwide and over 30 other countries such as Canada, China, Germany, Japan, and the United Kingdom.
What You Should Do
GE Healthcare began notifying customers of the issue via a formal letter on January 16, 2026. Healthcare facilities and providers using the affected versions of the Centricity Universal Viewer should follow the instructions provided in the firm's notification letter. For additional information or inquiries regarding the recall, customers may contact GE Healthcare at their Chicago office located at 500 W Monroe St, Chicago, IL 60661.
Why This Matters
This recall is critical because a mismatch between patient identification data and radiological images can lead to misdiagnosis or incorrect medical treatment, posing a significant risk to patient safety.
Source
FDA Recall Notification - Recall Number Z-1475-2026
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Frequently Asked Questions
Common questions about this FDA recall.