Device recall
Z-1635-2008: Integra LifeSciences Corporation Disposable Convenience Kit, PICC Insertion…
FDA device recall · Class II · Integra Pain Management
Key facts
| Recall number (Z-number) | Z-1635-2008 |
|---|---|
| Recall event | 47373 |
| Product | Integra LifeSciences Corporation Disposable Convenience Kit, PICC Insertion Tray, CUS791 |
| Product code | FMF |
| Recalling firm | Integra Pain Management |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 5, 2008 |
| 510(k) numbers | K960248 |
| FEI number | 1000138491 |
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