Bovie Medical Corporation recalls
Every recall we track for Bovie Medical Corporation — 11 in all, from 2018–2021 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Bovie Medical Corporation peaked in 2018 (6); 11 since 2017.
All FDA recall records for Bovie Medical Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 5 | 1 | 0 | 6 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 2 | 0 | 0 | 2 |
| 2021 | 0 | 0 | 3 | 0 | 3 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
What to do if you have a recalled Bovie Medical Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Bovie Medical Corporation recalls
4 shown- Lower riskMedical device
Bovie Medical Corporation recalls ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of
Bovie Medical recalls specific ConMed Disposable Bipolar Ablators due to potential pinholes in sterile packaging that could compromise sterility during surgery.
BovieFeb 1, 2021 - Use cautionMedical device
Bovie Medical Corporation recalls Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS,
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 MedicalApr 20, 2020 - Use cautionMedical device
Bovie Medical Corporation recalls J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of
Bovie recalls J-Plasma Precise 360 surgical handpieces from 2016 with potential PEEK tip separation risk. Learn about affected models and safety steps.
BovieJun 18, 2018 - Use cautionMedical device
Bovie Medical Corporation recalls J-Plasma Precise 360(R), Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR
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.
Bovie MedicalFeb 8, 2018
Bovie Medical Corporation recall questions
How many recalls has Bovie Medical Corporation had?
11 recalls from Bovie Medical Corporation are on record with U.S. safety agencies, from 2018–2021.
What is the most recent Bovie Medical Corporation recall?
Bovie Medical Corporation recalls ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of, dated Feb 1, 2021. Every Bovie Medical Corporation recall is listed on this page, newest first.
What should I do if I have a recalled Bovie Medical Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Bovie Medical Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.