Device recall
Z-1075-2015: The Plum A+ Infusion System is designed to meet the fluid delivery requirements…
FDA device recall · Class I · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1075-2015 |
|---|---|
| Recall event | 69336 |
| Product | The Plum A+ Infusion System is designed to meet the fluid delivery requirements of today's evolving healthcare environments. It is a cassette based multi-function infusion system. The Plum A+ allows two lines in and one line out. The pump can be used for standard, piggyback, or concurrent delivery… |
| Product code | FRN |
| Recalling firm | Hospira Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 24, 2017 |
| 510(k) numbers | K052052 |
| 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