Device recall
Z-1682-2017: Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of…
FDA device recall · Class II · Hospira Inc., A Pfizer Company
Key facts
| Recall number (Z-number) | Z-1682-2017 |
|---|---|
| Recall event | 76253 |
| Product | Plum 360 Infusion Pump, Software Version 15.02. The infusion pump is capable of delivering fluids for a variety of therapies such as parenteral, enteral, or epidural infusions |
| Product code | FRN |
| Recalling firm | Hospira Inc., A Pfizer Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 9, 2019 |
| 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