Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS Recalled by Bovie Medical Corporation Due to Unexpected stress fractures on the shaft of the...

Date: April 20, 2020
Company: Bovie Medical Corporation
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Bovie Medical Corporation directly.

Affected Products

Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS, APYX-044-BPS, APYX-150-BPP, and APYX-150-BPS - Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open surgical procedures.

Quantity: 13,948

Why Was This Recalled?

Unexpected stress fractures on the shaft of the hand piece may result in fragmentation during clinical use.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bovie Medical Corporation

Bovie Medical Corporation has 15 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report