FDA Adverse Event Injury Summary report: N

UTERINE ARTERY EMBOLIZATION

MDR report key: 1162723 · Received September 15, 2008

Report

Report Number
MW5008307
Event Type
Injury
Date Received
September 15, 2008
Date of Event
July 3, 2008
Report Date
September 15, 2008
Product Code
NAJ
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

THREE WEEKS POST UAE HAS A PELVIC SONOGRAM. THE NURSE WAS INFORMED THAT SHE CONTINUED TO HAVE VAGINAL FOUL SMELLING DISCHARGE. THE NURSE SAID IT WAS NORMAL. SHE CONTINUES TO HAVE FOUL SMELLING VAGINAL DISCHARGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UTERINE ARTERY EMBOLIZATION NONE NAJ

Patients

Seq Age Sex Outcome Treatment
1