FDA Adverse Event Injury Summary report: N

WOOD MASSAGE

MDR report key: 21949777 · Received May 2, 2025

Report

Report Number
MW5169789
Event Type
Injury
Date Received
May 2, 2025
Date of Event
January 20, 2025
Report Date
April 25, 2025
Manufacturer
UNK
Product Code
LYG
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

I BEEN HAVING MANY SERVICES (B)(6). I'VE TRIED CAVITATION, RED LIGHT THERAPY, WOOD MASSAGE. HOWEVER, THIS TIME SHE HAD TWO PERSONS FOR THE WOOD MASSAGE AND SHE USE THE SAME EQUIPMENT FOR BOTH WITHOUT CLEANING THE EQUIPMENT AND USE LEFTOVER MASSAGE OIL FROM THE OTHER PERSON ON ME, WHEN I SEE (B)(6) USING THE SAME EQUIPMENT, I TOLD HER TO STOP AND SHE SAID TO ME IT IS OKAY I ALWAYS USED THE SAME EQUIPMENT AND LEFTOVER OIL FOR THE PERSONS I SEE BACK TO BACK-- NOTHING HAPPENS. WHEN I GOT HOME, I HAD A RASH ALL OVER MY BODY WHERE SHE USE THE MASSAGE OIL, I HAD TO GO SEE A DOCTOR. SHE NEEDS TO BE CHECK SO OTHER PERSONS DON'T GET SICK FROM HER REUSING EQUIPMENT AND MESSAGE OILS. REF REPORTS: MW5169787, MW5169788.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1895306 WOOD MASSAGE MASSAGER, THERAPEUTIC, MANUAL LYG UNK

Patients

Seq Age Sex Outcome Treatment
1 41 YR Female