MAUDE Adverse Event Report: MEDTRONIC HEART VALVES DIVISION CG FUTURE BAND; RING, ANNULOPLASTY

Model Number 638RL30

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Mitral Regurgitation (1964)

Event Date 01/30/2020

Event Type  Injury  

Manufacturer Narrative

Product analysis: no product was returned.Conclusion: without the return of the product, no definitive conclusion can be made regarding the clinical observation.If information is provided in the future, a supplemental report will be issued.

Event Description

Medtronic received information that this patient presented to the hospital following non-st segment myocardial infarction (nstemi).Upon admission the patient required an intra-aortic balloon pump (iabp).The patient was then taken for emergent mitral valve surgery and coronary artery bypass grafting (cabg).The patient's native mitral valve had a torn papillary muscle resulting in a flail anterior and posterior leaflet and severe regurgitation.A medtronic mitral annuloplasty ring was used in conjunction with neochords in an attempt to repair the native mitral valve.It was reported that initially the repair appeared to be successful, but after removing the cross-clamp, moderate to severe residual mitral regurgitation was noted.As a result, the annuloplasty ring was explanted and replaced with a non-medtronic bioprosthetic valve.The patient was supported via venous-arterial extracorporeal membrane oxygenation (ecmo) and the pre-existing iabp at the conclusion of the operation.No additional adverse patient effects related to a medtronic device were reported. .

• Brand Name: CG FUTURE BAND
• Type of Device: RING, ANNULOPLASTY
• Manufacturer (Section D): MEDTRONIC HEART VALVES DIVISION; 1851 e deere ave; santa ana CA 92705
• Manufacturer (Section G): MEDTRONIC HEART VALVES DIVISION; 1851 e deere ave; santa ana CA 92705
• Manufacturer Contact: paula bixby ; 8200 coral sea street ne; mounds view, MN 55112 ; 7635055378
• MDR Report Key: 9827582
• MDR Text Key: 188623968
• Report Number: 2025587-2020-00766
• Device Sequence Number: 1
• Product Code: KRH
• UDI-Device Identifier: 00643169793538
• UDI-Public: 00643169793538
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K061127
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,health
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 03/12/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/12/2020
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 01/27/2024
• Device Model Number: 638RL30
• Device Catalogue Number: 638RL30
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 02/13/2020
• Date Device Manufactured: 01/28/2019
• 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: 54 YR