Device recall
Z-0973-05: Smith & Nephew Grasper, Cupped 3.4mm REF: 011014
FDA device recall · Class III · Smith & Nephew, Inc., Endoscopy Div.
Key facts
| Recall number (Z-number) | Z-0973-05 |
|---|---|
| Recall event | 32160 |
| Product | Smith & Nephew Grasper, Cupped 3.4mm REF: 011014 |
| Product code | GDJ |
| Recalling firm | Smith & Nephew, Inc., Endoscopy Div. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 7, 2006 |
| FEI number | 1219602 |
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