FDA Adverse Event Injury Summary report: N

NUFACE MICROCURRENT

MDR report key: 18783832 · Received February 23, 2024

Report

Report Number
MW5152002
Event Type
Injury
Date Received
February 23, 2024
Report Date
February 21, 2024
Manufacturer
CAROL COLE COMPANY
Product Code
NFO
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Description of Event or Problem · 0

WAS TREATED WITH DEVICE AND LATER THE SAME DAY DEVELOPED SYMPTOMS ASSOCIATED WITH RETINAL DETACHMENT IN THE RIGHT EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
119855 NUFACE MICROCURRENT STIMULATOR, TRANSCUTANEOUS ELECTRICAL, AESTHETIC PURPOSES NFO CAROL COLE COMPANY

Patients

Seq Age Sex Outcome Treatment
1 61 YR Female Other