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

Model Number	7700FB32
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	05/02/2022
Type of Reportable Event	Serious Injury
Additional 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 or Problem Description
Medtronic received information that during the implant of this 32mm mitral annuloplasty band, it was explanted and replaced with a 29mm non-medtronic mitral bioprosthetic valve.The reason for the replacement was reported to be due to a concern that the repair would result in mitral stenosis based on the presence of a rigid and thickened anterior leaflet.It was mentioned that the anterior mitral valve leaflet cleft was sutured closed and a posterior annuloplasty was performed using the 32mm mitral band.It was stated that despite the severe regurgitation having resolved, the anterior leaflet would not open and the band was then removed.No additional intervention or adverse patient effects were reported.

• Brand Name: SIMUPLUS BAND
• Common Device Name: 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: alison sweeney ; parkmore business park west; galway ; EI ; 091708096
• MDR Report Key: 14607540
• Report Number: 2025587-2022-01580
• Device Sequence Number: 12047156
• Product Code: KRH
• UDI-Device Identifier: 00763000271015
• UDI-Public: 00763000271015
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: K201449
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/06/2022

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: 09/02/2025
• Device Model Number: 7700FB32
• Device Catalogue Number: 7700FB32
• 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: 05/11/2022
• Initial Report FDA Received Date: 06/06/2022
• Date Device Manufactured: 09/14/2020
• 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
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 58 YR
• Patient Sex: Female