Device recall
Z-2061-2020: Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B, BVX-270B…
FDA device recall · Class II · Bovie Medical Corporation
Key facts
| Recall number (Z-number) | Z-2061-2020 |
|---|---|
| Recall event | 85597 |
| Product | Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B, BVX-270B, BVX-330B, BVX-270BPP, BVX- 330BPS, APYX-150B, APYX-270B, APYX-330B, APYX- 270BPP, and APYX-330BPS. Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open and laparoscopic surgical… |
| Product code | GEI |
| Recalling firm | Bovie Medical Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2022 |
| 510(k) numbers | K151325 |
| 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