MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION ADVANTAGE FIT? SYSTEM; MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC, FOR STRESS URINARY INCONTINENCE, RETR

Model Number	M0068502110
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	10/01/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Block b3 date of event: the exact event onset date is unknown.The provided event date of october 1, 2018, was chosen as the best estimate based on the date of the mesh removal surgery.Blocks d4, h4: the complainant was unable to provide the suspect device lot number; therefore, the lot expiration and device manufacture dates are unknown.Block h6: the patient code e2401 captures the reportable event of unspecified injury.The impact code f1903 captures the reportable event of mesh removal.
Event or Problem Description
It was reported that the patient implanted with the advantage fit system experienced an unspecified injury, leading to the mesh being explanted.The patient also underwent a robotic supracervical hysterectomy, bilateral salpingo-oophorectomy, sacrocolpopexy, enterocele repair, posterior repair, mid-urethral sling placement, and cystoscopy.
Additional Manufacturer Narrative
Block h2: additional information blocks a3a (sex), a3b (gender), and d4 (unique identifier (udi) #) has been updated based on the additional information received on march 30, 2025.Block b3 date of event: the exact event onset date is unknown.The provided event date of (b)(6) 2018, was chosen as the best estimate based on the date of the mesh removal surgery.Blocks d4, h4: the complainant was unable to provide the suspect device lot number; therefore, the lot expiration and device manufacture dates are unknown.Block h6: the patient code e2401 captures the reportable event of unspecified injury.The impact code f1903 captures the reportable event of mesh removal.
Event or Problem Description
It was reported that the patient implanted with the advantage fit system experienced an unspecified injury, leading to the mesh being explanted.The patient also underwent a robotic supracervical hysterectomy, bilateral salpingo-oophorectomy, sacrocolpopexy, enterocele repair, posterior repair, mid-urethral sling placement, and cystoscopy.

• Brand Name: ADVANTAGE FIT? SYSTEM
• Common Device Name: MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC, FOR STRESS URINARY INCONTINENCE, RETR
• Manufacturer (Section D): BOSTON SCIENTIFIC CORPORATION; 300 boston scientific way; marlborough MA 01752
• Manufacturer (Section G): BOSTON SCIENTIFIC CORPORATION; 780 brookside drive; spencer IN 47460
• Manufacturer Contact: farshad fahimi ; 4100 hamline avenue north; building c; saint paul, MN 55112
• MDR Report Key: 21611523
• Report Number: 2124215-2025-14833
• Device Sequence Number: 18067493
• Product Code: OTN
• UDI-Device Identifier: 08714729772880
• UDI-Public: (01)08714729772880
• Combination Product (Y/N): N
• Initial Reporter State: MN
• Initial Reporter Country: US
• PMA/510(K) Number: K020110
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Explanted Year: 2018
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/03/2025

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 Model Number: M0068502110
• Device Catalogue Number: M0068502110
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/19/2025
• Supplement Date Received by Manufacturer: 03/30/2025
• Initial Report FDA Received Date: 03/14/2025
• Supplement Report FDA Received Date: 04/03/2025
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female