Device recall
Z-1833-2016: The Plum A+ is a dual-line volumetric infusion system designed to meet the…
FDA device recall · Class II · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1833-2016 |
|---|---|
| Recall event | 73799 |
| Product | The Plum A+ is a dual-line volumetric infusion system designed to meet the growing demand for hospital-wide, as well as alternate site and home healthcare, standardization. With its primary line, secondary line, and piggyback fluid delivery capability, the Plum A+ is suited for a wide range of… |
| 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