MAUDE Adverse Event Report: COVIDIEN LP SURGIPRO; MESH, SURGICAL, POLYMERIC

Model Number	SPM-149
Medical Device Problem Codes	Migration or Expulsion of Device (1395); Mechanics Altered (2984); 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); Foreign Body Reaction (1868); Hematoma (1884); Hemorrhage/Blood Loss/Bleeding (1888); Hypersensitivity/Allergic reaction (1907); Unspecified Infection (1930); Inflammation (1932); Nausea (1970); Pain (1994); Perforation (2001); Scar Tissue (2060); Seroma (2069); Vomiting (2144); Hernia (2240); Discomfort (2330); Obstruction/Occlusion (2422); Ascites (2596); Unspecified Tissue Injury (4559); Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available (4581)
Type of Reportable Event	Serious Injury
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 a hernia.It was reported that after implant, the patient experienced infection, adhesion, pain, discomfort, mesh failure, defective device, mental pain, suffering, disability, impairment, and loss of enjoyment of life.Post-operative patient treatment included revision surgery, bowel resection, and mesh removal.
Additional Manufacturer Narrative
Additional info: a2 (date of birth), a3, a4, b5, b7, d6b, d10, h6 (patient codes, imf codes, device codes, ime e2402: "allergic reaction").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 a hernia.It was reported that after implant, the patient experienced mesh deformation/migration, recurrence, hematoma, inflammation, allergic reaction, obstruction, seroma, perforation, abscess, infection, adhesion, pain, discomfort, mesh failure, defective device, mental pain, suffering, disability, impairment, and loss of enjoyment of life.Post-operative patient treatment included medication, revision surgery, bowel resection, primary repair of ventral hernia, adhesiolysis, small bowel enterotomy closure, and mesh removal.
Additional Manufacturer Narrative
Additional info: h6 (patient codes, imf code, ime e2402 updated to include "fibroadipose tissue, serositis").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 a ventral hernia.It was reported that after implant, the patient experienced fluid collection, fibroadipose tissue, foreign body reaction, serositis, nausea, vomiting, scar tissue, small arterial bleeding vessel, mesh deformation/migration, recurrence, hematoma, inflammation, allergic reaction, obstruction, seroma, perforation, abscess, infection, adhesion, pain, discomfort, mesh failure, defective device, mental pain, suffering, disability, impairment, and loss of enjoyment of life.Post-operative patient treatment included drain placement for fluid collection, medication, revision surgery, bowel resection, primary repair of ventral hernia, adhesiolysis, small bowel enterotomy closure, removal of scar tissue, repair of small arterial bleeding vessel with suture, use of blake drains, and mesh removal.
Event or Problem Description
The patient¿s attorney alleged a deficiency against the device.The product was used for therapeutic treatment of a ventral hernia.It was reported that after implant, the patient experienced fluid collection, fibroadipose tissue, foreign body reaction, serositis, nausea, vomiting, scar tissue, small arterial bleeding vessel, mesh deformation/migration, recurrence, hematoma, inflammation, allergic reaction, obstruction, seroma, perforation, abscess, infection, adhesion, pain, discomfort, mesh failure, defective device, mental pain, suffering, disability, impairment, and loss of enjoyment of life.Post-operative patient treatment included drain placement for fluid collection, medication, revision surgery, bowel resection, primary repair of ventral hernia, adhesiolysis, small bowel enterotomy closure, removal of scar tissue, repair of small arterial bleeding vessel with suture, use of blake drains, mesh removal, removal of bowel (1/3 of intestines).
Additional Manufacturer Narrative
Additional information: 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.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: SURGIPRO
• Common Device Name: MESH, SURGICAL, POLYMERIC
• Manufacturer (Section D): COVIDIEN LP; 195 mcdermott rd; north haven CT 06473
• Manufacturer (Section G): COVIDIEN LP; 195 mcdermott rd; north haven CT 06473
• Manufacturer Contact: justin ellis ; 8200 coral sea st ne; mounds view, MN 55112 ; 7635265677
• MDR Report Key: 15294680
• Report Number: 1219930-2022-03325
• Device Sequence Number: 15011890
• Product Code: FTL
• UDI-Device Identifier: 10884521101333
• UDI-Public: 10884521101333
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K915526
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2003
• Device Explanted Year: 2005
• 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): 04/04/2024

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: SPM-149
• Device Catalogue Number: SPM-149
• Device Lot Number: A3E403
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/24/2022
• Supplement Date Received by Manufacturer: 07/19/2023; 01/17/2024; 03/27/2024
• Initial Report FDA Received Date: 08/25/2022
• Supplement Report FDA Received Date: 07/24/2023; 01/29/2024; 04/04/2024
• 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: VICRYL KNITTED/WOVEN MESH (ETHICON INC).
• Outcome Attributed to Adverse Event: Required Intervention; Disability
• Patient Sex: Female
• Patient Weight: 108 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: Black Or African American