Device recall
Z-0011-2010: AC Power Cords, shipped between 06/2005 and 05/2009. These cords were used in…
FDA device recall · Class II · Hospira Inc
Key facts
| Recall number (Z-number) | Z-0011-2010 |
|---|---|
| Recall event | 52866 |
| Product | AC Power Cords, shipped between 06/2005 and 05/2009. These cords were used in the following infusion pump models: Nutrimix, Q-Vue, Q2, Q2 Plus, Ox4, PCA, PCA II, PCA 3, Lifecare PCA, Lifecare 4100, Plum XL 3, Plum XL3M, Plum XL3D, Plum A+/ Plum A+3, and Gemstar Docking Station devices. AC cord… |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 30, 2010 |
| FEI number | 2921482 |
At a glance
- None 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