FDA Adverse Event Injury Summary report: N

ESSURE

MDR report key: 3983076 · Received August 6, 2014

Report

Report Number
MW5037595
Event Type
Injury
Date Received
August 6, 2014
Date of Event
October 14, 2013
Report Date
July 31, 2014
Manufacturer
BAYER
Product Code
HHS
Adverse Event
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT

Narratives

Description of Event or Problem · 1

(B)(4). I HAD SEVERE MENSTRUAL BLEEDING 18 DAY PERIODS..NUMBNESS IN TOES. HEADACHES AND FATIGUE..RESULTING IN A PARTIAL HYSTERECTOMY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
460994 ESSURE HHS BAYER

Patients

Seq Age Sex Outcome Treatment
1 37.000 YR Hospitalization