MAUDE Adverse Event Report: SOFRADIM PRODUCTION SAS PARIETEX; MESH, SURGICAL, POLYMERIC

Model Number	PCO2015X
Medical Device Problem Codes	Migration or Expulsion of Device (1395); Material Deformation (2976); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Abdominal Pain (1685); Adhesion(s) (1695); Pain (1994); Hernia (2240); Discomfort (2330); Injury (2348); Obstruction/Occlusion (2422); Ambulation or Postural Difficulties (2544); No Code Available (3191); Unspecified Gastrointestinal Problem (4491); Unspecified Tissue Injury (4559); Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Concomitant medical products: abstack30 abs fixation device 30 tacks (lot#n2d0684x); 174006 protack 5mm disp in (lot#p1g0856) ; abstack30 abs fixation device 30 tacks (lot#unknown).Patient codes-c64343 (massively dilated jejunum, small bowel torsion).If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an abdominal hernia.It was reported that after implant, the patient experienced hernia recurrence, adhesions, massive dilated jejunum, small bowel torsion, mesh pulled and mesh detachment.Post-operative patient treatment included revision surgery and bowel resection.
Additional Manufacturer Narrative
Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an abdominal hernia.It was reported that after implant, the patient experienced hernia recurrence, adhesions, massive dilated jejunum, small bowel torsion, mesh pulled and mesh detachment.Post-operative patient treatment included revision surgery and bowel resection.
Additional Manufacturer Narrative
Additional info: a4, b2 (added disability), b5, b7, h6 (updated all codes, added patient codes, device code, imf codes, and ime e2402: "small bowel torsion").Medtronic is submitting this report to comply with fda reporting regulations under 21 cfr parts 4 and 803.This report is based upon information obtained by medtronic, which the company may not have been able to fully investigate or verify prior to the date the report was required by the fda.Medtronic has made reasonable efforts to obtain more complete information and has provided as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.In particular, this report does not constitute an admission by anyone that the product described in this report has any ¿defects¿ or has ¿malfunctioned¿.These words are included in the fda 3500a form and are fixed items for selection created by the fda to categorize the type of event solely for the purpose of regulatory reporting.Medtronic objects to the use of these words and others like them because of the lack of definition and the connotations implied by these terms.This statement should be included with any information or report disclosed to the public under the freedom of information act.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an abdominal hernia.It was reported that after implant, the patient experienced abdominal pain, mesh deformation, mesh migration, fees like things are popping and moving, can't lift over 20lbs, can't climb stairs without getting winded, upset stomach, hernia recurrence, adhesions, massive dilated jejunum, small bowel torsion, mesh pulled and mesh detachment.Post-operative patient treatment included medication, revision surgery, lysis of adhesions, bowel resection and hernia repair with new mesh.
Additional Manufacturer Narrative
Additional information: a4, b5, b7, h6 (ime code).Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an abdominal hernia.It was reported that after implant, the patient experienced abdominal pain, mesh deformation, mesh migration, feels like things are popping and moving, can't lift over 20lbs, can't climb stairs without getting winded, upset stomach, hernia recurrence, adhesions, massive dilated jejunum, small bowel torsion, mesh pulled, mesh detachment, and pain.Post-operative patient treatment included medication, revision surgery, lysis of adhesions, bowel resection and hernia repair with new mesh.
Additional Manufacturer Narrative
Additional info: b2, b5, b6, b7, d4 (lot #), g1, h6 (patient codes), <(>&<)> additional codes.Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for a laparoscopic therapeutic treatment of an incisional ventral hernia.It was reported that after implant, the patient experienced abdominal pain, mesh deformation, mesh migration, feels like things are popping and moving, can't lift over 20lbs, can't climb stairs without getting winded, upset stomach, hernia recurrence, adhesions, massive dilated jejunum, small bowel torsion, mesh pulled, mesh detachment, pain, <(>&<)> slow return of bowel function.Post-operative patient treatment included medication, revision surgery, lysis of adhesions, bowel resection, hernia repair with new mesh, hospitalization, hernia sac excised, <(>&<)> mesh revision.
Additional Manufacturer Narrative
Additional info: a4, b7, g4 (510k #) medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: PARIETEX
• Common Device Name: MESH, SURGICAL, POLYMERIC
• Manufacturer (Section D): SOFRADIM PRODUCTION SAS; 116 avenue du formans; trevoux 01600 ; FR 01600
• Manufacturer (Section G): SOFRADIM PRODUCTION SAS; 116 avenue du formans; trevoux 01600 ; FR 01600
• Manufacturer Contact: mike bocchino ; 8200 coral sea st ne; 8200 coral sea st ne; mounds view,mn, CT 55112-4391 ; 8006464633
• MDR Report Key: 9616998
• Report Number: 9615742-2020-00142
• Device Sequence Number: 14122476
• Product Code: FTL
• UDI-Device Identifier: 10884521174689
• UDI-Public: 10884521174689
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K173796
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup,Followup,Followup
• Report Date (Section B): 10/24/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: PCO2015X
• Device Catalogue Number: PCO2015X
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/08/2020
• Supplement Date Received by Manufacturer: 01/05/2022; 12/13/2023; 01/22/2025; 08/13/2025; 10/22/2025
• Initial Report FDA Received Date: 01/22/2020
• Supplement Report FDA Received Date: 01/23/2022; 12/15/2023; 01/27/2025; 08/28/2025; 10/24/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE SECTION H10
• Outcome Attributed to Adverse Event: Disability; Required Intervention; Hospitalization
• Patient Sex: Male
• Patient Weight: 75 KG