Device recall
Z-2145-2012: Smith & Nephew 5.5 mm Dyonics Bonecutter,Electroblade Full Radius Part Number…
FDA device recall · Class II · Smith & Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-2145-2012 |
|---|---|
| Recall event | 62617 |
| Product | Smith & Nephew 5.5 mm Dyonics Bonecutter ,Electroblade Full Radius Part Number: 7205962 Product Usage: The Dyonics Electroblade Resector is indicated for use in arthroscopic surgical procedures of large and small articular cavities. The Dyonics Electroblade Resector is effective in soft and osseous… |
| Product code | GEI |
| Recalling firm | Smith & Nephew, Inc. Endoscopy Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 22, 2021 |
| 510(k) numbers | K012314 |
| FEI number | 3003604053 |
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