FDA Adverse Event Injury Summary report: N

TRANSSEPTAL NEEDLE, BRK SERIES

MDR report key: 24189541 · Received January 27, 2026

Report

Report Number
3008452825-2026-00021
Event Type
Injury
Date Received
January 27, 2026
Report Date
January 27, 2026
Manufacturer
ABBOTT MEDICAL
Product Code
DRC
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
EZ
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE RESULTS OF THE INVESTIGATION ARE INCONCLUSIVE SINCE THE DEVICE WAS NOT RETURNED FOR ANALYSIS. REVIEW OF THE DEVICE HISTORY RECORD WAS NOT POSSIBLE AS THE LOT NUMBER IS UNKNOWN. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED. MODEL/LOT NUMBER INFORMATION WAS NOT ABLE TO BE OBTAINED FOR THIS DEVICE. THEREFORE, FULL UDI INFORMATION(D4) AND 510K(G3) ARE NOT AVAILABLE.

Description of Event or Problem · 0

THE FOLLOWING WAS PUBLISHED IN JOURNAL OF INTERVENTIONAL CARDIOLOGY VOLUME 2025. WILEY. "ACUTE AND SHORT-TERM HEMODYNAMIC AND ECHOCARDIOGRAPHY CHANGES DURING AND AFTER LEFT ATRIAL APPENDAGE CLOSURE"; DALIBOR HERMAN. TWO CENTERS ENROLLED PATIENTS FOR LAAC FROM JANUARY 2022 TO JULY 2024. INVASIVE HEMODYNAMIC MEASUREMENTS OF LEFT ATRIAL PRESSURE (LAP) WERE TAKEN AFTER THE TRANSSEPTAL PUNCTURE AND POST DEVICE DEPLOYMENT (BOTH BEFORE AND AFTER ISOMETRIC EXERCISE). THE HEART FAILURE (HF) BIOMARKERS (NT-PROBNP, NT-PROANP, AND GDF-15) WERE ASSESSED BEFORE AND 3 MONTHS AFTER LAAC. THE ECHOCARDIOGRAPHIC PARAMETERS WERE ASSESSED BEFORE AND 6 MONTHS AFTER LAAC. TWO ADVERSE EVENTS OF PERICARDIAL EFFUSION WHICH REQUIRED PERICARDIOCENTESIS WERE REPORTED. BOTH PATIENTS RECOVERED WITH GOOD OUTCOMES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
247501 TRANSSEPTAL NEEDLE, BRK SERIES Trocar DRC ABBOTT MEDICAL

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Life Threatening| R