Device recall
Z-0798-06: FAST-FIX AB Curved Needle Delivery System, Used for meniscal repair. Product…
FDA device recall · Class II · Smith & Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-0798-06 |
|---|---|
| Recall event | 35033 |
| Product | FAST-FIX AB Curved Needle Delivery System, Used for meniscal repair. Product Number: 7209399 |
| Product code | KGS |
| Recalling firm | Smith & Nephew, Inc. Endoscopy Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2007 |
| 510(k) numbers | K020480 |
| FEI number | 3003604053 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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