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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Bovie Medical Corporation: 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.

Agency Publication Date: March 21, 2018
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Affected Products

Product: J-Plasma Precise(R) OPEN, Catalog Numbers: BVX-044-BPP, BVX-044-BPS, BVX-150-BPP, BVX-150-BPS

All lots manufactured since 01/01/2014

Product: J-Plasma Precise(R), Catalog Numbers: BVX-150B, BVX-150N, BVX-330B, BVX- 330N, BVX-450B, BVX-450N

All lots manufactured since 01/01/2014

Product: J-Plasma(R) Handpiece, Catalog Numbers: GS-018C, GS-270C, BVX-270B

All lots manufactured since 01/01/2014

Product: J-Plasma Precise 360(R), Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR

All lots manufactured since 01/01/2014

Product: J-Plasma Precise(R) FLEX, Catalog Number: BVX-500BF

All lots manufactured since 01/01/2014

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79398
Status: Resolved
Manufacturer: Bovie Medical Corporation
Manufactured In: United States
Units Affected: 5 products (1005 units; 6906 units; 5416 units; 595 units; 12 units)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.