MAUDE Adverse Event Report: MESH SUTRE, INC DURAMESH; SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE

Model Number	MSI-2015
Medical Device Problem Code	Improper or Incorrect Procedure or Method (2017)
Health Effect - Clinical Code	Wound Dehiscence (1154)
Date of Event	02/10/2023
Type of Reportable Event	Malfunction
Event or Problem Description
A review of the surgeon's report indicates that after using duramesh msi-2015 / lot #cb04pzb on a surgery performed (b)(6) 2023 the patient was observed on (b)(6) 2023 to require post-surgical intervention.The patient was admitted for an oncologic procedure and fascial closure with duramesh.The knots appeared to come unsecured post-surgery.Number of patients: 1.
Additional Manufacturer Narrative
The case was identified in the serious adverse events section of an interim registry report prepared by staff at (b)(6) university in preparation for journal publication in frontiers in surgery.Surgeon reported to manufacturer in a follow-up verbal interview that the device knot became unsecured due to only applying 3 throws, not alternating, a lapse in technique and user error.Post-surgical inquiry indicates patient has fully recovered.

• Brand Name: DURAMESH
• Common Device Name: SUTURE, NONABSORBABLE, SYNTHETIC, POLYPROPYLENE
• Manufacturer (Section D): MESH SUTRE, INC; 980 n. michigan ave; suite 1400; chicago IL 60611
• Manufacturer (Section G): MESH SUTURE, INC; 980 n. michigan ave; suite 1400; chicago IL 60611
• Manufacturer Contact: richard kearns ; 980 n. michigan ave; suite 1400; chicago, IL 60611 ; 2063902146
• MDR Report Key: 18351022
• Report Number: 3025431509-2023-00003
• Device Sequence Number: 6268658
• Product Code: GAW
• UDI-Device Identifier: 00850008298097
• UDI-Public: 00850008298097
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• PMA/510(K) Number: K211178
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Study
• Initial Reporter Occupation: Risk Manager
• Type of Report: Initial
• Report Date (Section B): 12/18/2023

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: MSI-2015
• Device Catalogue Number: MSI-2015
• Device Lot Number: CB04PZB
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/11/2023
• Initial Report FDA Received Date: 12/18/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 12/06/2022
• 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: Other
• Patient Age: 79 YR
• Patient Sex: Male
• Patient Weight: 77 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White