Bovie Medical Corporation: 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 procedures.

Recall number

Z-2061-2020

Recalling firm

Bovie Medical Corporation

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 procedures.

Status

Terminated

Initiated

2020-04-20

Posted

not on file

Terminated

2022-09-13

Reason

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

Root cause

Under Investigation by firm

Action

On April 23, 2020 Apyx Medical (Formerly Bovie Medical) sent out an URGENT Medical Device Field Safety Notice identifying the problem, under what circumstances it can occur, the actions that should be taken by the customer/user in order to prevent risk to patients/users, and the actions planned by Apyx Medical to correct the problem. PRODUCTS: All lots of the Renuvion/J-Plasma Precise Hand piece with specified Catlog #'s that are not expired, and all lots of the Renuvion/J-Plasma Precise Open Handpiece with specified Catlog #'s that are not expired. ACTIONS TO BE TAKEN BY CUSTOMER/USER: Follow the cleaning instructions provided in the Instructions for Use (IFU) to remove coagulum/eschar from the blade during clinical use: For optimum performance, keep the distal end of the shaft free of debris. A damp gauze pad can be used for cleaning. Do not activate while cleaning the tip. Follow all specified cleaning instructions identified in the Field Safety Notification which are also in the product Instructions for Use (IFU's). Do Not modify or alter the tip of the device. Do Not use a cannula or a skin port that has tight interference with the outer diameter of the shaft of the device. Discontinue using the hand piece if during clinical use if a stress fracture develops and immediately report to Apyx Medical for return if any devices that exhibit this issue during clinical use. Customers should sign and return the customer response form via email indicating they have read and understand the instructions by May 1st of 2020.

Quantity

38,738

Distribution

Worldwide distribution - US nationwide including in the states of Puerto Rico, and the countries of CA, JO, CO, MX, BR, CR, PA, KW, CL, MA, ES, TH, PH, IQ, LB, DO, Japan, QA, AE, PE, AU, VN, IL, Lithuania, UAE, Belgium, Denmark, Austria, Poland, Germany, Slovakia, Spain, Cyprus, Switzerland, Turkey, UK, Italy, Bulgaria, Greece, Norway, Ireland, Hungary, and Croatia.

Lot, serial or model codes

The following Catalog numbers which were distributed from 06/01/2016 through present: BVX-150B, BVX-270B, BVX-330B, BVX-270BPP, BVX- 330BPS, APYX-150B, APYX-270B, APYX-330B, APYX- 270BPP, APYX-330BPS

510(k) numbers

["K151325","K183160"]

PMA numbers

not on file

Product code

GEI

Firm FEI

3007593903

Firm city

Clearwater

Firm state

FL

Firm country

not on file

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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