MAUDE Adverse Event Report:; UTERINE ARTERY EMOLIZATION

; UTERINE ARTERY EMOLIZATION

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Device Problem Insufficient Information (3190)

Patient Problem Pain (1994)

Event Type Injury

Event Description

Chronic severe pain heaviness and back pain.She has been denied pain management.

1 Device was Involved in the Event
Type of Device	UTERINE ARTERY EMOLIZATION
MDR Report Key	3805732
MDR Text Key	4370021
Report Number	MW5036002
Device Sequence Number	1
Product Code	NAJ
Reporter Country Code	US
Number of Events Reported	1
Summary Report (Y/N)	N
Report Source	Voluntary
Reporter Occupation	Other Health Care Professional
Type of Report	Initial
Report Date	05/05/2014
1 Patient was Involved in the Event
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
Initial Date Manufacturer Received	Not provided
Initial Date FDA Received	05/06/2014
Patient Sequence Number	1
Patient Outcome(s)	Disability;