FDA Adverse Event Injury Summary report: N

TACTICATH¿ QUARTZ CONTACT FORCE ABLATION CATHETER

MDR report key: 8657914 · Received May 31, 2019

Report

Report Number
9680001-2019-00083
Event Type
Injury
Date Received
May 31, 2019
Report Date
May 31, 2019
Manufacturer
VENUSA DE MEXICO S.A. DE C.V.
Product Code
OAE
PMA / PMN Number
P130026
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

CONCOMITANT DEVICES: REFLEXION SPIRAL CATHETER, THERAPY COOL FLEX CATHETER, EVENT DATE UNKNOWN. 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. PER THE IFU, CARDIAC PERFORATION IS A KNOWN RISK DURING THE USE OF THIS DEVICE.

Description of Event or Problem · 1

RELATED MANUFACTURER REFERENCE NUMBER: 2182269-2019-00075, 2030404-2019-00037. THE FOLLOWING WAS PUBLISHED IN HEART AND VESSELS IN AN ARTICLE TITLED ¿COMPARISON BETWEEN NOVEL AND STANDARD HIGH-DENSITY 3D ELECTRO-ANATOMICAL MAPPING SYSTEMS FOR ABLATION OF ATRIAL TACHYCARDIA BY MAURY P, CHAMP-RIGOT L, ROLLIN A, WATTS T, ET AL., 09 NOVEMBER 2018. ¿SIXTY CONSECUTIVE ATRIAL TACHYCARDIA ABLATION PROCEDURES USING ULTRA-HIGH-DENSITY MAPPING (GROUP 1) WERE RETROSPECTIVELY COMPARED TO 60 CONSECUTIVE PROCEDURES USING STANDARD HIGH-DENSITY MAPPING (GROUP 2). MINOR COMPLICATIONS (NON-SURGICAL VASCULAR COMPLICATIONS OR ASYMPTOMATIC PERICARDIAL EFFUSIONS) OCCURRED IN 15 PATIENTS.¿ (HTTPS://DOI.ORG/10.1007/S00380-018-1307-1).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
451044 TACTICATH¿ QUARTZ CONTACT FORCE ABLATION CATHETER CARDIAC ABLATION PERCUTANEOUS CATHETER OAE VENUSA DE MEXICO S.A. DE C.V.

Patients

Seq Age Sex Outcome Treatment
1 Other