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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HERNIA MESH MESH, SURGICAL, POLYMERIC

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HERNIA MESH MESH, SURGICAL, POLYMERIC Back to Search Results
Device Problem Insufficient Information (3190)
Patient Problem Insufficient Information (4580)
Event Date 01/01/2007
Event Type  Injury  
Event Description

Dear medwatch, or to whom ever it may concern; i've contacted (b)(6), concerning representation in a double hernia mesh claim, with which i underwent surgery in 2007. I've been having complication since my surgery, but i've only been to the dr on two or three separate occasions for it since the 2007 surgery. (b)(6) attorneys decided not to represent me in this case, but advised me to not know any other law firms who handling hernia mesh cases. Then the (b)(6) attorneys advised me to contact your office for assistance, because you report serious reactions and problems with medical products, such as drugs and medical devices, and they also mentioned that i could also consult with your resource officer. I'm not sure what they mean about that. I would like to know is there anyway that your office can assist me in this matter, or know of any other law firms who may willing to assist me in this matter? and also i would like to know does your office have any other cases on medical products, medical devices, etc? thank you. I look forward to hearing from your office soon. (b)(6).

 
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Brand NameHERNIA MESH
Type of DeviceMESH, SURGICAL, POLYMERIC
MDR Report Key11702167
MDR Text Key246853935
Report NumberMW5100919
Device Sequence Number1
Product Code FTL
Combination Product (Y/N)
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation PATIENT
Type of Report Initial
Report Date 04/07/2021
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received04/20/2021
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? No
Device Operator NO INFORMATION
Was Device Available For Evaluation? No Answer Provided
Is The Reporter A Health Professional? No Answer Provided
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated By Manufacturer? No Answer Provided
Is The Device Single Use? No Answer Provided
Is this a Reprocessed and Reused Single-Use Device?
Type of Device Usage

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