Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a potential risk associated with the...
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, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparascopic surgical procedures.
Quantity: 1,176 total units
Why Was This Recalled?
There is a potential risk associated with the PEEK tip of the J-Plasma Precise 360 Handpiece separating from the handpiece and retained in the tissue.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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