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

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Pain (1994); Cramp(s) (2193); Discomfort (2330)

Event Type  No Answer Provided  

Event Description

My name is (b)(6).I am writing concerning a hernia mesh that was placed in me surgically.Ever since i have gotten sharp pain in my stomach, cramps and discomfort, also i get sharp pain in my stomach when ever i use the bathroom.Can i please get a list or something stating the side effects of hernia meshes.Also, please i would like to know if there is a list of lawyers that i can contact concerning my case of this hernia mesh.Please contact me as soon as you each time is limited.Thank you.

• Brand Name: HERNIA MESH
• Type of Device: MESH, SURGICAL, POLYMERIC
• MDR Report Key: 8883654
• MDR Text Key: 154314907
• Report Number: MW5088957
• Device Sequence Number: 1
• Product Code: FTL
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Patient
• Type of Report: Initial
• Report Date: 08/09/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/09/2019
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: No Information
• Was Device Evaluated by Manufacturer?: No Information
• Type of Device Usage: N
• Patient Sequence Number: 1