MAUDE Adverse Event Report: MEDTRONIC HEART VALVES DIVISION BAND 620BG23 DURAN ANCORE ANNULOPLASTY C; RING, ANNULOPLASTY

Model Number	620BG23
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Mitral Regurgitation (1964)
Date of Event	08/25/2020
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 23 mm mitral annuloplasty band, it was explanted and replaced with a 23 mm mitral annuloplasty band of the same model.It was reported that the reason for replacement was due to "significant mitral regurgitation".It was reported that the band was sutured along the annulus of the posterior leaflet.Leaflet augmentation was performed after the initial annuloplasty attempt, and no allegations were made against the annuloplasty band itself.No additional adverse patient effects were reported.

• Brand Name: BAND 620BG23 DURAN ANCORE ANNULOPLASTY C
• Common Device Name: RING, ANNULOPLASTY
• Manufacturer (Section D): MEDTRONIC HEART VALVES DIVISION; 1851 e deere ave; santa ana CA 92705
• MDR Report Key: 10636460
• Report Number: 2025587-2020-03026
• Device Sequence Number: 11420922
• Product Code: KRH
• UDI-Device Identifier: 00643169793439
• UDI-Public: 00643169793439
• Combination Product (Y/N): N
• Initial Reporter State: WV
• Initial Reporter Country: US
• PMA/510(K) Number: K032810
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/06/2020

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: 06/21/2025
• Device Model Number: 620BG23
• Device Catalogue Number: 620BG23
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/28/2020
• Initial Report FDA Received Date: 10/06/2020
• 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: 73 YR