Device recall
Z-2744-2020: Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re…
FDA device recall · Class II · Sutter Medizintechnik GmbH
Key facts
| Recall number (Z-number) | Z-2744-2020 |
|---|---|
| Recall event | 86035 |
| Product | Sutter Swyng non-stick bipolar forceps - Product Usage: single-use re electrosurgical instruments. The bipolar for-ceps are provided with bayonet-style handle design with straight or angled tips and different total lengths. They are to be connected through an appropriate bipolar cable with the… |
| Product code | GEI |
| Recalling firm | Sutter Medizintechnik GmbH |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 21, 2020 |
| 510(k) numbers | K193587 |
| FEI number | 3004857377 |
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