Device recall
Z-0128-2011: Hospira brand Symbiq Two-Channel Infuser, LIST No. 16027 Symbiq Two-Channel…
FDA device recall · Class I · Hospira Inc
Key facts
| Recall number (Z-number) | Z-0128-2011 |
|---|---|
| Recall event | 56462 |
| Product | Hospira brand Symbiq Two-Channel Infuser, LIST No. 16027 Symbiq Two-Channel Infuser, List Number Configurations: 16027-04-01/03/04, 51/52, 53/54, 79/80,81/82,83/84,87/88 and 89/90 16026-27-89/90, 16027-27-89/90, 16027-13-25/26,53/54, Distributed by: Hospira, Inc. Morgan Hill, CA |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 3, 2013 |
| 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