[Recalled] Centricity Universal Viewer Zero Footprint Client — Potential for Distance and Area measurements to display inaccurate measurement… | FDA 2022-04-28
Authorities recorded a safety problem with this product. The details below come directly from the government recall notice.
Recall details
| Product | Centricity Universal Viewer Zero Footprint Client |
|---|---|
| Brand / manufacturer | GE Healthcare, LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1229-2022 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 28 April 2022 |
| EAN / barcode | 00840682102988 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Potential for Distance and Area measurements to display inaccurate measurement values when performed on magnified images, and specific to ZFP, Distance and Area measurements can display inaccurate measurement values when performed on lossy images that are scaled down from their original resolution.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from GE Healthcare, LLC
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.