Device recall
Z-0944-2009: Symbiq One-Channel list number 16026-04 and Two-Channel list number 16027-04…
FDA device recall · Class II · Hospira Inc
Key facts
| Recall number (Z-number) | Z-0944-2009 |
|---|---|
| Recall event | 50541 |
| Product | Symbiq One-Channel list number 16026-04 and Two-Channel list number 16027-04 Infusion System, a general purpose infuser, Distributed and Manufactured by Hospira Inc, Morgan Hill, CA. Is a general purpose infuser designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes… |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 3, 2012 |
| 510(k) numbers | K041550 |
| FEI number | 2921482 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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