Device recall
Z-0727-04: PatientNet Monitoring System - PatientNet Central Stations utilizing software…
FDA device recall · Class II · General Electric Medical Systems Information Technology
Key facts
| Recall number (Z-number) | Z-0727-04 |
|---|---|
| Recall event | 28410 |
| Product | PatientNet Monitoring System - PatientNet Central Stations utilizing software Versions 1.03.14, 1.04xx, 2.00xx. |
| Product code | MSX |
| Recalling firm | General Electric Medical Systems Information Technology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 17, 2005 |
| 510(k) numbers | K020524 |
| FEI number | 2124823 |
At a glance
- 1–9 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