Device recall
Z-0704-04: Endocoupler, C-Mount 30 mm Focal Length Catalog Number: 7204823, 7204823S
FDA device recall · Class II · Smith And Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-0704-04 |
|---|---|
| Recall event | 28423 |
| Product | Endocoupler, C-Mount 30 mm Focal Length Catalog Number: 7204823, 7204823S |
| Product code | FXM |
| Recalling firm | Smith And Nephew, Inc. Endoscopy Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 28, 2006 |
| FEI number | 3003604053 |
At a glance
- None 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