Device recall
Z-1482-2014: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including…
FDA device recall · Class I · Hospira Inc.
Key facts
| Recall number (Z-number) | Z-1482-2014 |
|---|---|
| Recall event | 67591 |
| Product | Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions including whole blood or red blood cell components and enteral fluids using a wide variety of standard administration sets and fluid containers. |
| Product code | FRN |
| Recalling firm | Hospira Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 16, 2017 |
| 510(k) numbers | K991501 |
| 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