Every recall we track for Bovie Medical Corporation — 11 in all — plus the complaints and injury reports the public filed about them.
Bovie Medical recalls HNM Disposable Bipolar Ablators with potential pinholes in sterile packaging that could breach sterility during surgery. Affected units have specific catalog numbers and lots.
Bovie Medical recalls Velocity Disposable Bipolar Ablators with potential pinholes in sterile packaging that could breach sterility during surgery. Affected units include specific catalog numbers and lots. Consumers should contact Bovie for details.
Bovie Medical recalls specific ConMed Disposable Bipolar Ablators due to potential pinholes in sterile packaging that could compromise sterility during surgery.
Bovie Medical recalls Renuvion/J-Plasma handpieces with catalog numbers BVX-150B to APYX-330BPS due to potential shaft fractures during surgery. Affected devices may fragment, causing injury.
Bovie Medical recalls Renuvion handpieces with specific catalog numbers due to potential shaft fractures during surgery. Affected models were sold from June 2016 onward. Contact for return instructions.
Bovie recalls J-Plasma Precise 360 surgical handpieces from 2016 with potential PEEK tip separation risk. Learn about affected models and safety steps.
Bovie Medical recalls J-Plasma Precise OPEN devices with specific catalog numbers and production dates due to risk of patient fluid backflow and cross-contamination if generator is reused.
Bovie Medical recalls J-Plasma handpieces with catalog numbers GS-018C, GS-270C, BVX-270B made since January 2014 due to incomplete cable plug insertion causing potential cross-contamination if generator is reused.
Bovie Medical recalls J-Plasma Precise FLEX devices (BVX-500BF) made since Jan 2014 due to incomplete cable plug insertion causing potential cross-contamination if reused.
Bovie Medical recalls J-Plasma Precise devices with specific catalog numbers and production dates due to risk of patient fluid backflow and cross-contamination if generator is reused.
Bovie Medical recalls J-Plasma Precise 360(R) devices with specific catalog numbers and production dates due to risk of patient fluid backflow and cross-contamination if the generator is reused.
