FDA Enforcement
Class II
Terminated
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.
Recall: Z-2648-2016
·
Reported August 31, 2016
Enforcement
- Recall Number
- Z-2648-2016
- Event ID
- 74790
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Bovie Medical Corporation
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- August 31, 2016
- Initiation Date
- July 18, 2016
- Classification Date
- August 24, 2016
- Termination Date
- December 14, 2016
- Address
- 5115 Ulmerton Rd, Clearwater, FL, 33760-4004, United States
Description
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.
Reason
The adhesive may be inadequately applied or the assembly may be manipulated after application of the adhesive resulting in an incomplete bond to the angled tip.
Code Info
Lot 0316D.
Distribution
Worldwide Distribution - US Nationwide in the states of: MD, GA, MO and FL and the country of Finland.
Quantity
95