FDA Adverse Event Malfunction Summary report: N

TENDRIL STS

MDR report key: 20248440 · Received September 18, 2024

Report

Report Number
2017865-2024-65259
Event Type
Malfunction
Date Received
September 18, 2024
Report Date
September 18, 2024
Manufacturer
ST. JUDE MEDICAL, INC.(CRM-SYLMAR)
Product Code
NVN
UDI-DI
05414734502887
PMA / PMN Number
P960013
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE INITIAL INFORMATION WAS OBTAINED FROM THE ARTICLE TITLED "BRADYCARDIA-DEPENDENT CONDUCTION BLOCK OF THE ATRIAL TISSUE IN A PATIENT AFTER DOUBLE-CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR IMPLANTATION. JOURNAL OF ELECTROCARDIOLOGY 86 (2024) 153776. HTTPS://DOI.ORG/10.1016/J.JELECTROCARD.2024.153776.¿ AUTHORS: KAILUN ZHU, ZHANXIONG ZHENG, YANXI SHI, JIANJIANG XU, ZHENLIANG CHU A,D, DEPARTMENT OF CARDIOLOGY, THE SECOND AFFILIATED HOSPITAL OF JIAXING UNIVERSITY, JIAXING, ZHEJIANG 314000, CHINA B MEDICAL COLLEGE OF YANGZHOU UNIVERSITY, YANGZHOU, JIANGSU 225009, CHINA C DEPARTMENT OF CARDIOLOGY, JIANGSU TAIZHOU PEOPLE¿S HOSPITAL, TAIZHOU, JIANGSU 225300, CHINA D DEPARTMENT OF CARDIOLOGY, THE FIRST AFFILIATED HOSPITAL OF DALIAN MEDICAL UNIVERSITY, DALIAN, LIAONING 116000, CHINA

Description of Event or Problem · 0

INFORMATION ORIGINATING FROM PEER REVIEW ARTICLE: IT WAS REPORTED THAT PARTIAL ATRIAL LOSS OF CAPTURE, HIGH CAPTURE THRESHOLD AND PSEUDO-ATRIAL FUSION WAS OBSERVED POST IMPLANT WAS OBSERVED ON THE IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ICD) AND RIGHT ATRIAL (RA) LEAD POST IMPLANT. PROGRAMMING CHANGES WERE MADE. THE ICD AND RA LEAD REMAINED IMPLANTED AND IN USE FOLLOWING THE PROGRAMMING CHANGES. THE PATIENT WAS STABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1302732 TENDRIL STS No Match NVN ST. JUDE MEDICAL, INC.(CRM-SYLMAR) 2088TC/52 P000128702 05414734502887

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown TENDRIL STS