FDA Adverse Event Injury Summary report: N

ALWAYS MAXI PADS OVERNIGHT

MDR report key: 23405460 · Received October 28, 2025

Report

Report Number
MW5178109
Event Type
Injury
Date Received
October 28, 2025
Date of Event
October 2, 2025
Report Date
October 23, 2025
Manufacturer
UNK
Product Code
HHL
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
WI, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

ALWAYS MAXI PADS (OVERNIGHT SIZE) AND POSSIBLY TAMPONS; SYMPTOMS DECREASED WITH TAMPON USE IN PLACE OF MAXI PAD BUT DIDN'T SUBSIDE/DISAPPEAR. THE DATE OF (B)(6) 2025 WAS MY INITIAL VAGINAL EXAM WITH A FULL STD PANEL AT (B)(6), TO FIGURE OUT WHAT WAS CAUSING THE IRRITATION; I WENT TO MY PRIMARY DOCTORS OFFICE THE VERY NEXT DAY FOR A SECOND OPINION AND QUICKER RESULTS. RESULTS SHOWED NO YEAST INFECTION, NO POSITIVE STD/STI (SEXUALLY TRANSMITTED DISEASES/SEXUALLY TRANSMITTED INFECTIONS) RESULTS (I CAN PROVIDE PROOF OF THIS VISIT AND RESULTS IF NEEDED). SINCE MY CYCLE ENDED A FEW WEEKS AGO TO TODAY, I'VE HAD NONE OF THE SYMPTOMS MINUS SLIGHT VAGINAL DRYNESS ON MY LABIA. REASON FOR USE: MENSTRUAL CYCLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
213857 ALWAYS MAXI PADS OVERNIGHT PAD, MENSTRUAL, SCENTED HHL UNK

Patients

Seq Age Sex Outcome Treatment
1 33 YR Female Required Intervention| L| O ADDERALL IR.| ADDERALL XR.