Device recall
Z-2381-2010: Hospira Inc. Symbiq One- and Two- Channel Infuser, List Numbers 16026 and 16027…
FDA device recall · Class I · Hospira Inc
Key facts
| Recall number (Z-number) | Z-2381-2010 |
|---|---|
| Recall event | 56523 |
| Product | Hospira Inc. Symbiq One- and Two- Channel Infuser, List Numbers 16026 and 16027 respectively. |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 30, 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