Device recall
Z-0454-2014: The GE Centricity Web; Software Version 3.0x, is intended for use under the…
FDA device recall · Class II · Ge Healthcare It
Key facts
| Recall number (Z-number) | Z-0454-2014 |
|---|---|
| Recall event | 64762 |
| 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… |
| Product code | LMD |
| Recalling firm | Ge Healthcare It |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 13, 2017 |
| FEI number | 3004526608 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database