Device recall
Z-1129-2007: Curlin Medical Administration Sets: Model Numbers 340-4111, IV Administration…
FDA device recall · Class II · Curlin Medical Llc
Key facts
| Recall number (Z-number) | Z-1129-2007 |
|---|---|
| Recall event | 38341 |
| Product | Curlin Medical Administration Sets: Model Numbers 340-4111, IV Administration Sets. |
| Product code | FPA |
| Recalling firm | Curlin Medical Llc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2008 |
| 510(k) numbers | K981816 |
| FEI number | 3002936294 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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