Device recall
Z-1561-2009: Smith & Nephew Endoscopic Disposable Blades: STONECUTTER ACR,4.0,EP-1,DSP Part…
FDA device recall · Class II · Smith & Nephew, Inc. Endoscopy Division
Key facts
| Recall number (Z-number) | Z-1561-2009 |
|---|---|
| Recall event | 52042 |
| Product | Smith & Nephew Endoscopic Disposable Blades: STONECUTTER ACR,4.0,EP-1,DSP Part #: 7205330. DYONICS Series 3000 BONECUTTER Disposable Arthroscopic Surgery Blades are indicated for resection of soft and osseous tissues in large and small articular cavities. Specific applications may include knee and… |
| Product code | NBH |
| Recalling firm | Smith & Nephew, Inc. Endoscopy Division |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| FEI number | 3003604053 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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