Device recall
Z-0021-2010: Plum LifeCare 5000 (Plum 1.6) with Dataport, list #s 02507-04-11, 02507-04-51…
FDA device recall · Class II · Hospira Inc
Key facts
| Recall number (Z-number) | Z-0021-2010 |
|---|---|
| Recall event | 52866 |
| Product | Plum LifeCare 5000 (Plum 1.6) with Dataport, list #s 02507-04-11, 02507-04-51; AC cord manufactured by Electri-Cord, Westfield PA, Infusion pumps manufactured by Hospira, Morgan Hill, CA. |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2010 |
| 510(k) numbers | K911401 |
| FEI number | 2921482 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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