MAUDE Adverse Event Report: DAVOL INC., SUB. C.R. BARD, INC. -1213643 XENMATRIX; PORCINE SURGICAL MESH

Catalog Number	1161935
Medical Device Problem Code	Patient-Device Incompatibility (2682)
Health Effect - Clinical Code	Hernia (2240)
Date of Event	09/22/2015
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
As reported, post implant of the xenmatrix, the patient was diagnosed with hernia recurrence and underwent reoperation for mesh removal.The clinician has assessed the patient¿s postoperative course as "possibly" related related to the study device and not related to the procedure.However, based on the information provided, no conclusion can be made.Hernia recurrence is known inherent risk of surgery.The instructions-for-use (ifu) supplied with the device lists hernia recurrence as a possible complication.Review of manufacturing records confirms product was manufactured to specification.This mdr represent the ae of hernia recurrence.An additional mdr was submitted to represent the event of fistula.Not returned - mesh explanted.
Event or Problem Description
Alleged per clinical trial (b)(4): on (b)(6) 2014, the patient underwent multiple recurrent ventral suprapubic open hernia repair procedure during which a xenmatrix surgical graft was trimmed and placed in underlay fashion inter peritoneally, fixated using sutures.Fascia was completely closed using suture through interrupted stitch.Full skin closure was achieved using sutures.Concomitant procedure includes lysis of adhesion(s).The patient was discharged to home on (b)(6) 2014.On (b)(6) 2014, the patient underwent removal of jackson pratt drain and discharged on the same day.On (b)(6) 2014, the patient was diagnosed with fistula; the spontaneous draining sinus resolved over time on (b)(6) 2015, patient underwent physical exam during which ventral suprapubic hernia (3.7 cm2) was diagnosed and confirmed through ct scan on (b)(6) 2015.On (b)(6) 2015 patient underwent an additional surgery and the device was explanted.The fascia was completely closed using suture through interrupted stitch and the skin was fully closed.The patient was discharged on (b)(6) 2015.The ae is clinically assessed to be of moderate severity, possibly related to the study device and not related to the procedure and recovered/resolved.The reported adverse event meets the definition of an sae (serious adverse event).

• Brand Name: XENMATRIX
• Common Device Name: PORCINE SURGICAL MESH
• Manufacturer (Section D): DAVOL INC., SUB. C.R. BARD, INC. -1213643; 100 crossings blvd.; warwick RI 02886
• Manufacturer (Section G): BARD SHANNON LIMITED -3005636544; san geronimo industrial park; lot #1, road #3, km 79.7; humacao PR 00791
• Manufacturer Contact: andrew topoulos ; 100 crossings blvd.; warwick, RI 02886 ; 8005566756
• MDR Report Key: 15188629
• Report Number: 1213643-2022-00576
• Device Sequence Number: 5634101
• Product Code: FTM
• UDI-Device Identifier: 00801741031441
• UDI-Public: (01)00801741031441
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: K140501
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2015
• Reporter Type: Manufacturer
• Report Source: Other,Study,Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 07/26/2022

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: 04/30/2016
• Device Catalogue Number: 1161935
• Device Lot Number: HUYD1101
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/21/2022
• Initial Report FDA Received Date: 08/08/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 05/13/2014
• 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: Hospitalization; Required Intervention
• Patient Age: 28 YR
• Patient Sex: Female
• Patient Weight: 87 KG