Device recall
Z-2807-2011: ***EXPANDED RECALL*** Curlin Infusion Administration Set, REF 340-4119, Sterile…
FDA device recall · Class II · Zevex International, Inc.
Key facts
| Recall number (Z-number) | Z-2807-2011 |
|---|---|
| Recall event | 57829 |
| Product | ***EXPANDED RECALL*** Curlin Infusion Administration Set, REF 340-4119, Sterile EO, Zevex, Inc., 4314 Zevex Park Lane, Salt Lake City, UT 84123. The Curlin Ambulatory Infusion Pump System with disposable PVC Administration Tubing Sets and user accessories, provide a means for the volumetric delivery… |
| Product code | FRN |
| Recalling firm | Zevex International, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 27, 2011 |
| 510(k) numbers | K981816 |
| FEI number | 1000117172 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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