• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BAYER ESSURE

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

BAYER ESSURE Back to Search Results
Event Date 10/27/2014
Event Type  Death  
Event Description

(b)(4). Found out i was pregnant with the essure stuck in my uterus.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameESSURE
Manufacturer (Section D)
BAYER
MDR Report Key4936434
Report NumberMW5044663
Device Sequence Number1
Product CodeHHS
Report Source Voluntary
Source Type Invalid data
Reporter Occupation Patient
Type of Report Initial
Report Date 06/24/2015
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received07/23/2015
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator Service Personnel
Is The Reporter A Health Professional? No
Was Device Evaluated By Manufacturer? No Answer Provided
Type of Device Usage Invalid Data

Patient TREATMENT DATA
Date Received: 07/23/2015 Patient Sequence Number: 1
Treatment
GABAPENTINLEXAPROIRON
-
-