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 |