Device recall
Z-1832-2016: The Plum 360 is a large volume infuser capable of delivering fluids for a…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1832-2016 |
|---|---|
| Recall event | 73799 |
| Product | The Plum 360 is a large volume infuser capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions. The Plum 360 infuser can deliver fluids over a broad range of infusion rates and is capable of Concurrent delivery from one or more rigid or flexible… |
| Product code | FRN |
| Recalling firm | Hospira Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 6, 2018 |
| 510(k) numbers | K141789 |
| FEI number | 3013319212 |
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