MAUDE Adverse Event Report: AZIYO BIOLOGICS, INC. TYKE; PATCH, PLEDGET, INTRACARDIAC - DXZ

Model Number CMCV-098-204

Device Problem Off-Label Use (1494)

Patient Problems Mitral Valve Stenosis (1965); Mitral Valve Insufficiency/ Regurgitation (4451)

Event Type  Injury  

Manufacturer Narrative

Manufacturing review of the cormatrix tyke device history record could not be completed as the lot number was not provided.No specific treatment dates were provided aside from patients records selected for this retrospective review occurred between may 2013 and october 2017, however, the tyke product was not released for distribution until may 2016.Information cited in the article states that "patients underwent a mitral valve replacement using the tyke ecm patch to form a custom-made cylinder mitral valve replacement".The instructions for use (art-20712a) provided with the distributed product states under warnings and precautions that "tyke is not indicated for the construction or replacement of total valves or conduits".Although the exact cause of the reported issues cannot be conclusively determined, the reported worsening valve stenosis and/or regurgitation are identified in the instructions for use as potential complications provided with the tyke product.Should aziyo receive any additional details related to this event, a supplemental report will be filed.

Event Description

As part of the post market surveillance process, this retrospective single center, single surgeon study report published in pediatric cardiology titled "mitral valve replacement in pediatrics using an extracellular matrix cylinder valve: a case series" was reviewed.This article summarizes the results of eight (8) children under the age of 2 years who underwent ecm custom-made cylinder valves for mitral valve replacement.The study states that these patients were treated between march 2013 and october 2017 using the cormatrix (now aziyo biologics) tyke 2-ply extracellular matrix material (model # / lot #: unknown).This report is focused on patient #4 as referenced in table 1: summary table of the eight patients who initially underwent mitral valve repair however under direct inspection, the surgeon determined repair was not feasible and mitral valve replacement was performed.Patient #4 was identified with congenital mv arcade/stenosis and underwent ecm-mvr at the age of 3 months.At 5 months post-op, the patient underwent balloon valvuloplasty due to a mean mitral valve gradient of 18mmhg.At 7.9 months (237 days) post ecm-mvr replacement, this patient required further surgery to implant a replacement mitral valve (melody valve) and explanting the ecm mitral valve.Attempts to contact the corresponding author have been successful at this time, however, should any additional information be received a follow-up report will be filed.

• Brand Name: TYKE
• Type of Device: PATCH, PLEDGET, INTRACARDIAC - DXZ
• Manufacturer (Section D): AZIYO BIOLOGICS, INC.; 1100 old ellis road; ste 1200; roswell GA 30076
• Manufacturer (Section G): AZIYO BIOLOGICS, INC.; 1100 old ellis road; ste 1200; roswell GA 30076
• Manufacturer Contact: michael hennick ; 1100 old ellis road; ste 1200; roswell, GA 30076
• MDR Report Key: 10955949
• MDR Text Key: 219889045
• Report Number: 3005619880-2020-00102
• Device Sequence Number: 1
• Product Code: DXZ
• UDI-Device Identifier: 00859389005102
• UDI-Public: 00859389005102
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K152127
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: literature
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 12/06/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/06/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: CMCV-098-204
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 11/06/2020
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 3 MO
• Patient Weight: 4