Device recall
Z-1415-04: ADP2.1 Adapter, non-sterile reusable Model Number: 30-802-1,an accessory used…
FDA device recall · Class II · TissueLink Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1415-04 |
|---|---|
| Recall event | 29697 |
| Product | ADP2.1 Adapter, non-sterile reusable Model Number: 30-802-1 ,an accessory used with the TissueLink BiPolar Floating Device |
| Product code | GEI |
| Recalling firm | TissueLink Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 4, 2004 |
| 510(k) numbers | K020574, K022532 |
| FEI number | 1000517638 |
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