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

Model Number	PPM4530
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Adhesion(s) (1695); Emotional Changes (1831); High Blood Pressure/ Hypertension (1908); Unspecified Infection (1930); Necrosis (1971); Pain (1994); Renal Failure (2041); Seroma (2069); Hernia (2240); Ulcer (2274); Deformity/ Disfigurement (2360); Impaired Healing (2378); Respiratory Failure (2484); Unspecified Tissue Injury (4559); Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Type of Reportable Event	Death
Additional Manufacturer Narrative
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 incisional hernia.It was reported that after implant, the patient experienced mental pain, physical deformity, disability, impairment, loss of enjoyment of life, disfigurement, mental anguish, pain, necrotic tissue, and death.Post-operative patient treatment included icu visit, intubation, sedation, necrotic tissue debridement, wound vac, and revision surgery.Information received indicates the patient is deceased.No information was provided regarding the circumstances of expiration.
Additional Manufacturer Narrative
Additional info: a1, a4, a5b, b2, b5, b6, b7, d10, <(>&<)> h6 (patient codes, ime e2402: leukocytosis) 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 incisional hernia.It was reported that after implant, the patient experienced skin ulceration, hypertension, abdominal compartment syndrome, recurrence, infection, mental pain, physical deformity, disability, impairment, loss of enjoyment of life, disfigurement, mental anguish, pain, necrotic tissue, kidney failure, respiratory failure, leukocytosis, wound infection, <(>&<)> death.Post-operative patient treatment included mesh removal, icu visit, intubation, sedation, necrotic tissue debridement, wound vac, revision surgery, <(>&<)> hospitalization.Information received indicates the patient is deceased.No information was provided regarding the circumstances of expiration.
Additional Manufacturer Narrative
Additional info: ime e2402: "abdominal compartment syndrome").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 incisional hernia.It was reported that after implant, the patient experienced skin ulceration, hypertension, abdominal compartment syndrome, recurrence, infection, mental pain, physical deformity, disability, impairment, loss of enjoyment of life, disfigurement, mental anguish, pain, necrotic tissue, and death.Post-operative patient treatment included mesh removal, icu visit, intubation, sedation, necrotic tissue debridement, wound vac, and revision surgery.Information received indicates the patient is deceased.No information was provided regarding the circumstances of expiration.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of an incisional hernia.It was reported that after implant, the patient experienced adhesions, seroma, improper wound healing, skin ulceration, hypertension, abdominal compartment syndrome, recurrence, infection, mental pain, physical deformity, disability, impairment, loss of enjoyment of life, disfigurement, mental anguish, pain, necrotic tissue, kidney failure, respiratory failure, leukocytosis, wound infection, <(>&<)> death.Post-operative patient treatment included mesh removal, icu visit, intubation, sedation, necrotic tissue debridement, wound vac, revision surgery, <(>&<)> hospitalization.Information received indicates the patient is deceased.No information was provided regarding the circumstances of expiration.
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.

• Brand Name: PARIETENE
• 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: justin ellis ; 8200 coral sea st ne; mounds view, MN 55112 ; 7635265677
• MDR Report Key: 16040565
• Report Number: 9615742-2022-01218
• Device Sequence Number: 5306993
• Product Code: FTL
• UDI-Device Identifier: 10884521213791
• UDI-Public: 10884521213791
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K142091
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• 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
• Report Date (Section B): 10/31/2023

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 Model Number: PPM4530
• Device Catalogue Number: PPM4530
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/07/2022
• Supplement Date Received by Manufacturer: 08/09/2023; 08/23/2023; 10/25/2023
• Initial Report FDA Received Date: 12/22/2022
• Supplement Report FDA Received Date: 08/10/2023; 08/30/2023; 10/31/2023
• 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: 12X12 IN VICRYL MESH
• Outcome Attributed to Adverse Event: Disability; Hospitalization; Life Threatening; Death; Required Intervention
• Patient Sex: Female
• Patient Weight: 99 KG
• Patient Race: White