Device recall
Z-1181-2008: Hospira LifeCare PCA Label Utility, Version 1.0 CD. The installation/user guide…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1181-2008 |
|---|---|
| Recall event | 46846 |
| Product | Hospira LifeCare PCA Label Utility, Version 1.0 CD. The installation/user guide is entitled "LifeCare PCA Barcode Label Utility Program." This software program is designed to allow entry of each drug concentration into a formulation library on a pharmacy computer for standardized printing of barcode… |
| Product code | MEA |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 9, 2010 |
| FEI number | 3013319212 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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