PlainRecalls

Bovie Medical Corporation

15 recalls on record · Latest: Mar 10, 2021

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Agency notice ledger

Federal filing book Bovie Medical Corporation LIGHT-BOOK · SINGLE-AGENCY

#1,014 of 14,151 · 15 notices · 0.014% archive

  • BOOK 15 notices
  • RANK #1,014 of 14,151
  • SHARE 0.014% archive
  • AGENCY FDA Devices (15)
  • CAT medical devices
  • CATS 1 category
  • LATEST Mar 10, 2021
  • PHOTO Acumed LLC

Nearest notice-volume peer: Acumed LLC (0 notice gap)

Bovie Medical Corporation accounts for about 0.014% of the 104,423-notice archive on 15 distinct filings — a mid share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where Bovie Medical Corporation sits among 14,151 recalling firms

Bovie Medical Corporation ranks 1,014th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

Bovie Medical Corporation vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

15 1014th of 14151 higher than 13,088 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

Bovie Medical Corporation in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows Bovie Medical Corporation holds about 0.014% of archive notices alongside 15 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
FDA Devices Moderate Mar 10, 2021

ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

FDA Devices Moderate Mar 10, 2021

Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

FDA Devices Moderate Mar 10, 2021

HNM Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

FDA Devices Moderate May 27, 2020

Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS, APYX-044-BPS, APYX-150-BPP, and APYX-150-BPS - Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open surgical procedures.

FDA Devices Moderate May 27, 2020

Renuvion/ J-Plasma Precise Handpiece. Catalog numbers BVX-150B, BVX-270B, BVX-330B, BVX-270BPP, BVX- 330BPS, APYX-150B, APYX-270B, APYX-330B, APYX- 270BPP, and APYX-330BPS. Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open and laparoscopic surgical procedures.

FDA Devices Moderate Oct 31, 2018

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.

FDA Devices Moderate Mar 28, 2018

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

FDA Devices Moderate Mar 28, 2018

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

FDA Devices Moderate Mar 28, 2018

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

FDA Devices Moderate Mar 28, 2018

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

FDA Devices Moderate Mar 28, 2018

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

FDA Devices Moderate Aug 31, 2016

BVX-450NR Bovie Precise 360 Handpiece 45cm, needle Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.

FDA Devices Moderate Aug 31, 2016

BVX-330BR Bovie Precise 360 Handpiece 33cm, blade Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.

FDA Devices Moderate Aug 31, 2016

BVX-450BR Bovie Precise 360 Handpiece 45cm, blade Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.

FDA Devices Moderate Aug 31, 2016

BVX-330NR Bovie Precise 360 Handpiece 33cm, needle Product is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparoscopic surgical procedures.

Bovie Medical Corporation holds a measurable archive slice

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Frequently Asked Questions

How many federal recall notices name Bovie Medical Corporation?
PlainRecalls indexes 15 distinct federal recall events naming Bovie Medical Corporation, aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does Bovie Medical Corporation sit among other recalling firms?
Bovie Medical Corporation ranks #1,014 of 14,151 by distinct recall-event count among 14,151 firms in this archive (92nd percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of Bovie Medical Corporation's notices?
FDA Devices accounts for 15 of this firm's 15 indexed notices.
What product category dominates Bovie Medical Corporation's filing book?
Filings for Bovie Medical Corporation span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous?
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
Bovie Medical Corporation: 15 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming Bovie Medical Corporation; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026