Device recall
Z-0685-2007: Plicator EPS Plication System Catalog Number: 160-01128R
FDA device recall · Class II · NDO Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-0685-2007 |
|---|---|
| Recall event | 37247 |
| Product | Plicator EPS Plication System Catalog Number: 160-01128R |
| Product code | KOG |
| Recalling firm | NDO Surgical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2007 |
| 510(k) numbers | K032820 |
| FEI number | 3003309251 |
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