FDA Adverse Event Death Summary report: N

MITRACLIP CLIP DELIVERY SYSTEM

MDR report key: 10351109 · Received July 31, 2020

Report

Report Number
2024168-2020-06366
Event Type
Death
Date Received
July 31, 2020
Date of Event
May 31, 2020
Report Date
July 31, 2020
Manufacturer
ABBOTT VASCULAR
Product Code
NKM
PMA / PMN Number
P100009
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICES WERE NOT RETURNED FOR ANALYSIS AND A REVIEW OF THE LOT HISTORY RECORD AND SIMILAR COMPLAINT REVIEW COULD NOT BE PERFORMED AS THE PART AND LOT INFORMATION REGARDING THE COMPLAINT DEVICES WAS NOT PROVIDED. BASED ON THE INFORMATION PROVIDED A CONCLUSIVE CAUSE FOR THE REPORTED DEATH CANNOT BE DETERMINED. THE REPORTED PATIENT EFFECT OF DEATH, AS LISTED IN THE MITRACLIP SYSTEM INSTRUCTIONS FOR USE, IS A KNOWN POSSIBLE COMPLICATION ASSOCIATED WITH MITRACLIP PROCEDURES. THERE IS NO INDICATION OF A PRODUCT ISSUE WITH RESPECT TO MANUFACTURE, DESIGN, OR LABELING. ARTICLE TITLED, OUTCOMES OF URGENT/EMERGENT TRANSCATHETER MITRAL VALVE REPAIR (MITRACLIP): A SINGLE CENTER EXPERIENCE.

Description of Event or Problem · 1

THIS IS FILED TO REPORT DEATH. IT WAS REPORTED THROUGH A RESEARCH ARTICLE THAT FROM JANUARY 2018 TO MARCH 2019, 20 PATIENT PATIENTS UNDERWENT URGENT/EMERGENT TRANSCATHETER MITRAL VALVE REPAIR WITH A MITRACLIP. OVER THE 14-MONTH PERIOD, THE MITRACLIP MAY HAVE CONTRIBUTED TO DEATH. DETAILS ARE LISTED IN THE ARTICLE, TITLED ¿OUTCOMES OF URGENT/EMERGENT TRANSCATHETER MITRAL VALVE REPAIR (MITRACLIP): A SINGLE CENTER EXPERIENCE.¿ NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
814295 MITRACLIP CLIP DELIVERY SYSTEM VALVE REPAIR NKM ABBOTT VASCULAR

Patients

Seq Age Sex Outcome Treatment
1 72 YR Death