Device recall
Z-2239-2010: The Starion Instruments Thermal Ligating Shears 35C Model 102-138D and 23C Model…
FDA device recall · Class II · Starion Instruments
Key facts
| Recall number (Z-number) | Z-2239-2010 |
|---|---|
| Recall event | 55043 |
| Product | The Starion Instruments Thermal Ligating Shears 35C Model 102-138D and 23C Model numbers 102-137D allow the surgeon to position the distal jaws of the instrument around the region of tissue to be cut/cauterized. The surgeon squeezes the handle and depresses the switch, heating elements activates in… |
| Product code | GEI |
| Recalling firm | Starion Instruments |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 27, 2010 |
| 510(k) numbers | K062257 |
| FEI number | 1000137656 |
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