Device recall
Z-2648-2016: BVX-450BR Bovie Precise 360 Handpiece 45cm, blade Product is used for the…
FDA device recall · Class II · Bovie Medical Corporation
Key facts
| Recall number (Z-number) | Z-2648-2016 |
|---|---|
| Recall event | 74790 |
| Product | BVX-450BR Bovie Precise 360 Handpiece 45cm, blade Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures. |
| Product code | GEI |
| Recalling firm | Bovie Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 14, 2016 |
| 510(k) numbers | K152570 |
| FEI number | 3007593903 |
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