Device recall
Z-1816-2009: Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel…
FDA device recall · Class II · Hospira Inc
Key facts
| Recall number (Z-number) | Z-1816-2009 |
|---|---|
| Recall event | 52523 |
| Product | Hospira Phoenix Infusion System with MedNet Software, Symbiq Two-Channel Infusion System, Software versions v2.1 & v3.0, Manufactured by Hospira Inc., Morgan Hill, CA |
| Product code | frn |
| Recalling firm | Hospira Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 18, 2010 |
| 510(k) numbers | K041550 |
| FEI number | 2921482 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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