Device recall
Z-1410-2017: The UNI-CP System; Model Number: 330230SND.
FDA device recall · Class III · Integra LifeSciences Corp.
Key facts
| Recall number (Z-number) | Z-1410-2017 |
|---|---|
| Recall event | 76408 |
| Product | The UNI-CP System; Model Number: 330230SND. |
| Product code | JDR |
| Recalling firm | Integra LifeSciences Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 8, 2017 |
| 510(k) numbers | K011716 |
| FEI number | 3003418325 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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