Device recall
Z-0070-2013: Symbiq Two Channel Infuser; an Rx medical device infusion pump used to…
FDA device recall · Class I · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-0070-2013 |
|---|---|
| Recall event | 63056 |
| Product | Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospira, Inc., Lake Forest, IL 60045 USA, Made in Costa Rica; List Number 16027-01 Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals… |
| Product code | FRN |
| Recalling firm | Hospira Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 15, 2017 |
| 510(k) numbers | K041550 |
| FEI number | 3013319212 |
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