FDA Adverse Event Injury Summary report: N

BREAST TRACER

MDR report key: 24152030 · Received January 22, 2026

Report

Report Number
MW5182648
Event Type
Injury
Date Received
January 22, 2026
Report Date
January 15, 2026
Manufacturer
UNK
Product Code
PUV
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
FL, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

THERE WAS A TRACER PLACED IN MY BREAST BACK IN (B)(6) 2011. THE FINDINGS WERE BENIGN, THE TRACER WAS PUT IN BY (B)(6), I'VE MADE SEVERAL ATTEMPTS TO REACH OUT TO THEM BECAUSE I WANT THE TRACER REMOVED, THEY GAVE LITTLE TO KNOW INFORMATION OF THE PROCEDURE EVER BEING DONE. IT IS NOW CAUSING UNUSUAL SENSATIONS WITHIN MY BODY AND THINNING OF MY HAIR. ANY SUPPORT YOU CAN PROVIDE TO SOLVE THIS ISSUE WOULD BE GREATLY APPRECIATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
215583 BREAST TRACER LYMPH NODE LOCATION SYSTEM DURING SENTINEL BIOPSY PROCEDURE PUV UNK

Patients

Seq Age Sex Outcome Treatment
1 60 YR Female Other MORINGA.| NEFEDIPINE.| OIL OF OREGANO.| OMEGA +TUMERIC.| VITAMIN D-3 + K2.