[Recalled] The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity Enterprise Web is an image and information distribution system for the clinical
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| Product | The GE Centricity Web; Software Version 3.0x, is intended for use under the direct supervision of a licensed healthcare practitioner. The Centricity Enterprise Web is an image and information distribution system for the clinical review of medical images and reports. The Centricity Enterprise Web is |
|---|---|
| Brand / manufacturer | Ge Healthcare It |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-0454-2014 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 19 April 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: GE Healthcare has become aware of an issue associated with rejected images using the WADO protocol within GE Centricity Web that may impact patient safety. The WADO (Web Access to DICOM Objects) interface allows for embedding DICOM images as JPEGs on a web page and is available as a licensed operation on Centricity Web. When rejected images are archived by Centricity PACS to Enterprise Archive, an
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 It
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.