Device recall
Z-1277-2013: Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage…
FDA device recall · Class II · Olympus America Inc.
Key facts
| Recall number (Z-number) | Z-1277-2013 |
|---|---|
| Recall event | 64935 |
| Product | Olympus SurgMaster UES-40 electrosurgical unit ("UES-40") Product Usage: Designed for use in a medical facility under the supervision of a trained physician. It has been designed for general (open) and endoscopic surgery including urology, gynecology, respiratory and gastroenterology in conjunction… |
| Product code | KNS |
| Recalling firm | Olympus America Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 5, 2013 |
| 510(k) numbers | K030194 |
| FEI number | 2429304 |
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