FDA Adverse Event Malfunction Summary report: N

ESSURE

MDR report key: 2771821 · Received September 28, 2012

Report

Report Number
MW5027141
Event Type
Malfunction
Date Received
September 28, 2012
Report Date
September 26, 2012
Manufacturer
CONCEPTUS INC.
Product Code
HHS
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
CA, US
Reporter Occupation
OTHER CAREGIVERS

Narratives

Description of Event or Problem · 1

ESSURE PERMANENT BIRTH CONTROL IMPLANTED WITH POSITIVE PREGNANCIES: SIX CASES IDENTIFIED (B)(6) 2012.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ESSURE ESSURE PERMANENT BIRTH CONTROL HHS CONCEPTUS INC. ESS-305 810890

Patients

Seq Age Sex Outcome Treatment
1