FDA Adverse Event Injury Summary report: N

ALWAYS SANITARY NAPKIN

MDR report key: 1990010 · Received February 9, 2011

Report

Report Number
MW5019379
Event Type
Injury
Date Received
February 9, 2011
Report Date
February 9, 2011
Product Code
HHD
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
KY, US
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

TO WHOM IT MAY CONCERN, IT IS MY UNDERSTANDING THAT YOU ARE CURRENTLY CONSIDERING PLACING WARNINGS ON BOXES OF POWDERED LATEX GLOVES. I URGE YOU TO DO SO. MY SON, (B)(6) AND I HAVE BOTH BEEN DIAGNOSED WITH LATEX ALLERGY IN THE PAST YR AND A HALF. NEITHER OF US ARE HEALTHCARE WORKERS NOR HAVE SPINA BIFIDA. I WORKED FOR A BRIEF TIME IN FOOD SERVICE IN MY EARLY 20'S BUT HAVE NOT HELD JOBS, THAT I REMEMBER, WHERE I WAS SIGNIFICANTLY EXPOSED. I WAS DIAGNOSED AFTER PROGRESSIVELY WORSENING REACTIONS TO A MAINSTREAM BRAND OF SANITARY NAPKINS AND THANKFULLY THOSE REACTIONS STOPPED WHEN I SWITCHED TO A BRAND THAT IS LISTED ON THE LATEX-FREE LISTS PROVIDED BY VARIOUS ORGANIZATIONS AND ASSOCIATIONS. YRS AGO, I HAD TRANSIENT SKIN IRRITATION AND RASHES AFTER USING RUBBER GLOVES FOR DISH WASHING. I NOW HAVE TYPE 1 LATEX ALLERGY REACTIONS/SYMPTOMS. I URGE YOU TO PLACE WARNINGS ON THE GLOVES BECAUSE POWDERED LATEX GLOVE USE HAS DELAYED MY MEDICAL CARE. I RECENTLY ASKED AN ENDOCRINOLOGIST TO RE-EVALUATE ME FOR TYPE 1 DIABETES BUT BECAUSE OF POWDERED GLOVE USE, AND LACK OF UNDERSTANDING OF THIS ALLERGY AND THE RISKS THAT POWDERED GLOVES POSE, I HAVE HAD TO EDUCATE THEIR OFFICE AND ADVOCATE FOR MYSELF AND DELAY TREATMENT UNTIL ACCOMMODATIONS COULD BE MADE. AS IT IS, I STILL AM NOT ABLE TO GET LABWORK DONE IN THEIR OFFICE AND HAVE TO USE MY PRIMARY CARE'S OFFICE LAB, ALL BECAUSE OF POWDERED GLOVE USE AND THE CROSS-CONTAMINATION THAT COMES WITH IT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ALWAYS SANITARY NAPKIN SANITARY NAPKIN HHD

Patients

Seq Age Sex Outcome Treatment
1 41 YR Life Threatening| O