Device recall
Z-2681-2017: The Plum A+ Infusion Systems are a multipurpose family of devices that provides…
FDA device recall · Class II · ICU
Key facts
| Recall number (Z-number) | Z-2681-2017 |
|---|---|
| Recall event | 64542 |
| Product | The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel… |
| Product code | FRN |
| Recalling firm | ICU |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 31, 2018 |
| 510(k) numbers | K070398 |
| 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