MAUDE Adverse Event Report: ENDOMETRIAL ABLATION

ENDOMETRIAL ABLATION

Device Problem Insufficient Information (3190)

Patient Problem No Code Available (3191)

Event Date 09/05/2012

Event Type Injury

Event Description

Endometrial ablation resulted in infertility.She would like to know if it's possible to rebuild her uterus so that she can conceive.

1 Device was Involved in the Event
Brand Name	ENDOMETRIAL ABLATION
Type of Device	ENDOMETRIAL ABLATION
MDR Report Key	5105090
MDR Text Key	26832929
Report Number	MW5056517
Device Sequence Number	1
Product Code	HHR
Number of Events Reported	1
Summary Report (Y/N)	N
Report Source	Voluntary
Reporter Occupation	Other
Report Date	09/21/2015
1 Patient was Involved in the Event
Date FDA Received	09/21/2015
Is this an Adverse Event Report?	Yes
Is this a Product Problem Report?	No
Device Operator	Health Professional
Is the Reporter a Health Professional?	Yes
Type of Device Usage	N
Patient Sequence Number	1
Patient Outcome(s)	Other;