Device recall
Z-2076-2012: Alaris PC unit model 8015 Product Usage: The device is labeled for prescription…
FDA device recall · Class I · CareFusion 303, Inc.
Key facts
| Recall number (Z-number) | Z-2076-2012 |
|---|---|
| Recall event | 62007 |
| Product | Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only. |
| Product code | FRN |
| Recalling firm | CareFusion 303, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 13, 2014 |
| 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