Device recall
Z-2211-2010: DATEX-OHMEDA NETWORK AND ICENTRAL '05, SALES REVISION 4.3 ( Datek-Ohmeda Network…
FDA device recall · Class II · Ge Healthcare, Llc
Key facts
| Recall number (Z-number) | Z-2211-2010 |
|---|---|
| Recall event | 55502 |
| Product | DATEX-OHMEDA NETWORK AND ICENTRAL '05, SALES REVISION 4.3 ( Datek-Ohmeda Network and iCentral (including iCentral Client)) The Datex-Ohmeda Network and iCentral (including iCentral Client) transfers information between networked Datex-Ohmeda devices in the Monitor Network as well as between Monitor… |
| Product code | MSX |
| Recalling firm | Ge Healthcare, Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 14, 2012 |
| 510(k) numbers | K052972 |
| FEI number | 2126677 |
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