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 |