Device recall
Z-2011-2012: Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX…
FDA device recall · Class II · Stingray Surgical Products, LLC
Key facts
| Recall number (Z-number) | Z-2011-2012 |
|---|---|
| Recall event | 62024 |
| Product | Bipolar Forceps model number: S02-XXX, S03-XXX, P02-XXX, and P03-XXX. "Instructions For Use" (QF7.5.1A.R01 thru QF7.5.1A.R06 Care and Handling of Bipolar Forceps. Bipolar Forceps designed to grasp, manipulate and coagulate selected tissue for use in general surgical procedures powered by a high… |
| Product code | GEI |
| Recalling firm | Stingray Surgical Products, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 6, 2014 |
| 510(k) numbers | K083162 |
| FEI number | 3006059917 |
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