Device recall
Z-1870-2011: Curlin PainSmart IOD Ambulatory Infusion Pump Provides a means for the…
FDA device recall · Class I · Zevex International, Inc.
Key facts
| Recall number (Z-number) | Z-1870-2011 |
|---|---|
| Recall event | 57939 |
| Product | Curlin PainSmart IOD Ambulatory Infusion Pump Provides a means for the volumetric delivery of fluids used in Parenteral, Enteral, Epidural, Subcutaneous and Intravenous applications. |
| Product code | FRN |
| Recalling firm | Zevex International, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 6, 2012 |
| 510(k) numbers | K981816 |
| FEI number | 1000117172 |
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