Device recall
Z-1204-2012: The Reprocessed Mitek Arthroscopic Wand is considered a soft tissue ablators…
FDA device recall · Class II · Stryker Sustainability Solutions, Inc.
Key facts
| Recall number (Z-number) | Z-1204-2012 |
|---|---|
| Recall event | 61296 |
| Product | The Reprocessed Mitek Arthroscopic Wand is considered a soft tissue ablators. Soft tissue ablators are radiofrequency (RF) surgical tools designed for removal and dissection of tissue in arthroscopic surgeries. A generator or controller serves as the power unit. Soft tissue ablators are available in… |
| Product code | GEI |
| Recalling firm | Stryker Sustainability Solutions, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2012 |
| 510(k) numbers | K012695 |
| FEI number | 1000132435 |
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