MAUDE Adverse Event Report: MEDTRONIC HEART VALVES DIVISION BAND 620BG29 DURAN ANCORE ANNULOPLASTY C; RING, ANNULOPLASTY

Model Number	620B
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Codes	Mitral Regurgitation (1964); Mitral Valve Prolapse (2471); No Information (3190)
Date of Event	01/25/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Product analysis: the product specimen has not been returned for device analysis.Conclusion: multiple attempts to gather additional information and request product return have been made; however, these attempts have been unsuccessful.Without return of the product, no definitive conclusions could be drawn regarding the clinical observation.Should the device be returned or additional information become available, a supplemental report will be submitted.A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
Medtronic received information that immediately post implant of this annuloplasty ring in the mitral position, this device was explanted and replaced.No failure mechanism and no other adverse patient effects were reported.
Additional Manufacturer Narrative
Additional information was received that after the patient had the annuloplasty band implanted, the patient still exhibited severe mitral regurgitation and leaflet prolapse.The physician then decided to explant the band and implant a 27mm bioprosthetic mitral valve.
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.

• Brand Name: BAND 620BG29 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: 6404529
• Report Number: 2025587-2017-00403
• Device Sequence Number: 552766
• Product Code: KRH
• UDI-Device Identifier: 00613994759108
• UDI-Public: 00613994759108
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K032810
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 08/14/2017

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: 09/14/2021
• Device Model Number: 620B
• Device Catalogue Number: 620BG29
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 02/24/2017
• Supplement Date Received by Manufacturer: 08/14/2017; 08/14/2017
• Initial Report FDA Received Date: 03/14/2017
• Supplement Report FDA Received Date: 08/14/2017; 09/06/2017
• 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: 70 YR
• Patient Weight: 70