FDA Adverse Event Injury Summary report: N

J-PLASMA

MDR report key: 7014689 · Received November 9, 2017

Report

Report Number
3007593903-2017-00009
Event Type
Injury
Date Received
November 9, 2017
Report Date
November 9, 2017
Manufacturer
BOVIE MEDICAL CORPORATION
Product Code
GEI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

PATIENT IS EXPERIENCING PROLONGED HEALING TIME AFTER FACIAL RESURFACING WITH J-PLASMA PROCEDURE.

Description of Event or Problem · 1

PATIENT EXPERIENCING PROLONGED HEALING AFTER FACIAL RESURFACING WITH J-PLASMA.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
794783 J-PLASMA J-PLASMA HANDPIECE, GEI BOVIE MEDICAL CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention