FDA Adverse Event Injury Summary report: N

BREATHE RIGHT

MDR report key: 3815303 · Received May 12, 2014

Report

Report Number
MW5036101
Event Type
Injury
Date Received
May 12, 2014
Report Date
May 9, 2014
Product Code
LWF
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

I USED A BREATHE RIGHT STRIP THAT CLAIMED TO BE "LATEX FREE." I HAD A SERIOUS ALLERGIC REACTION INCLUDING DIARRHEA AND NAUSEA. THE PRODUCT IS NOT LATEX FREE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
284854 BREATHE RIGHT BREATHE RIGHT LWF

Patients

Seq Age Sex Outcome Treatment
1 Other