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

Model Number	PCO3020X
Medical Device Problem Codes	Migration or Expulsion of Device (1395); Adverse Event Without Identified Device or Use Problem (2993); Patient Device Interaction Problem (4001)
Health Effect - Clinical Codes	Abscess (1690); Adhesion(s) (1695); Emotional Changes (1831); Hemorrhage/Blood Loss/Bleeding (1888); Unspecified Infection (1930); Necrosis (1971); Pain (1994); Perforation (2001); Seroma (2069); Hernia (2240); Impaired Healing (2378); Abdominal Distention (2601); Fluid Discharge (2686); Thrombosis/Thrombus (4440); Unspecified Tissue Injury (4559)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Note: acknowledge the discrepancy between the manufactured date and the reported implant date.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 therapeutic treatment of hernia.It was reported that after implant, the patient experienced recurrence, infection, abscess, adhesions, pain, open wound.Post-operative patient treatment included revision surgery, removal of mesh, wound vac.
Additional Manufacturer Narrative
Additional information: a2 (date of birth), a3a, a4, b5, b7, d4 (udi #), d6a, h4, h6 (patient codes, imf codes, device 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 therapeutic treatment of hernia.It was reported that after implant, the patient experienced bleeding, seroma, perforation, abdominal distention, hernia incarceration, necrosis, mesh retraction, blood clot, emotional injuries, recurrence, infection, abscess, adhesions, pain, chronic open draining wound.Post-operative patient treatment included medication, incision and drainage, debridement, exploratory laparotomy, resection of skin and wound, enterolysis, abdominal washout, bowel resection, bowel repair, revision surgery, removal of mesh, and wound vac.

• 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 55112-4391 ; 8006464633
• MDR Report Key: 19639353
• Report Number: 9615742-2024-00907
• Device Sequence Number: 8793580
• Product Code: FTL
• UDI-Device Identifier: 10884521179851
• UDI-Public: (01)10884521179851(17)240930(10)PTJ1906M
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K173796
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/01/2025

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?: No
• Operator of Device: Health Professional
• Device Expiration Date: 09/30/2024
• Device Model Number: PCO3020X
• Device Catalogue Number: PCO3020X
• Device Lot Number: PTJ1906M
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/26/2024
• Supplement Date Received by Manufacturer: 11/19/2025
• Initial Report FDA Received Date: 06/28/2024
• Supplement Report FDA Received Date: 12/01/2025
• Date Device Manufactured: 10/20/2019
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Male
• Patient Weight: 109 KG