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.
- Company
- Bovie Medical Corporation
- Recall Initiated
- June 18, 2018
- Terminated
- April 8, 2019
- Recall Number
- Z-0198-2019
- Quantity
- 1,176 total units
- Firm Location
- Clearwater, FL
Reason for Recall
There is a potential risk associated with the PEEK tip of the J-Plasma Precise 360 Handpiece separating from the handpiece and retained in the tissue.
Distribution
Worldwide Distribution: US (nationwide) to states of:: CA, CO, FL, ID, IL, MD, MO, NJ, NY, OH, OR, PA,, TX.; and countries of: Austria, Bahrain, Belgium, Bulgaria, Cyprus, Finland, Great Britain, Hungary, Ireland, Israel, Italy, Qatar, Scandinavia, Slovakia, Switzerland, Turkey, and United Arab Emirates.
Lot / Code Info
Catalog Numbers: BVX-330BR, BVX-330NR, BVX-450BR, BVX-450NR. All lot number are included that have been manufactured since 05/01/2016.
Root Cause
Nonconforming Material/Component
Action Taken
The firm, Bovie Medical, notified customers regarding the recall on or about 06/18/2018 via a letter entitled "URGENT: MEDICAL DEVICE RECALL". The letter alerted customers to discontinue to use the device with the affected catalog and lot numbers, to return the impacted handpieces to Bovie Medical, to consider using a device which did not contain the defective component, and how to receive a replacement device. Bovie Medical indicated the resolution to this issue will be a manufacturing and/or design change to the affected handpieces. The letter also stated to complete and return the response form included with the letter within ten(10) days by email to corrections@boviemed.com or by fax to the Regulatory Affairs Department at (727) 388-4697. Questions and comments can be directed to corrections@boviemed.com or call toll free 1-800-537-2790, Monday through Friday, 8:00 AM to 5:00 PM, Eastern Time.