Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
J-Plasma Precise 360(R) Recalled by Bovie Medical Corporation Due to Bovie Medical is issuing a correction to address...
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
J-Plasma Precise 360(R), Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR
Quantity: 595 units
Why Was This Recalled?
Bovie Medical is issuing a correction to address incomplete insertion of the J-Plasma(R) handpiece cable plug into the generator receptacle resulting in an incomplete helium seal. The potential exists for patient fluid backflow into the handpiece and the generator receptacle leading to risk of cross-contamination if the generator is reused.
Where Was This Sold?
worldwide
About Bovie Medical Corporation
Bovie Medical Corporation has 15 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report