Device recall
Z-0492-2011: Alaris PC unit Model 8000 only when used with Alaris Pump module or Alaris…
FDA device recall · Class II · CareFusion Corporation
Key facts
| Recall number (Z-number) | Z-0492-2011 |
|---|---|
| Recall event | 56405 |
| Product | Alaris PC unit Model 8000 only when used with Alaris Pump module or Alaris Syringe module |
| Product code | FRN |
| Recalling firm | CareFusion Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2013 |
| 510(k) numbers | K051641 |
| FEI number | 2016493 |
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