Device recall
Z-0389-06: Hospira brand Plum A+I.V. Infusion Pump, List No. 11971-04; Hospira brand Plum…
FDA device recall · Class II · Hospira Inc
Key facts
| Recall number (Z-number) | Z-0389-06 |
|---|---|
| Recall event | 32077 |
| Product | Hospira brand Plum A+I.V. Infusion Pump, List No. 11971-04; Hospira brand Plum A+I.V. Infusion Pump, List No. 12391-04; Hospira brand Plum A+3 I.V. Infusion Pump, List No. 12618-04; Hospira brand Plum A+3 I.V. Infusion Pump, List No. 12348-04; Infusion pump is a multi-function fluid delivery… |
| Product code | FRN |
| Recalling firm | Hospira Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 21, 2006 |
| FEI number | 2921482 |
At a glance
- None 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