FDA Adverse Event Injury Summary report: N

THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER

MDR report key: 3163470 · Received June 11, 2013

Report

Report Number
9673241-2013-00189
Event Type
Injury
Date Received
June 11, 2013
Date of Event
May 16, 2013
Report Date
June 6, 2013
Manufacturer
BIOSENSE WEBSTER, INC. (JUAREZ)
Product Code
LPB
PMA / PMN Number
P030031/S025
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

MULTIPLE ATTEMPTS HAVE BEEN MADE TO REQUEST FOR THE COMPLAINT PRODUCT TO BE RETURNED FOR ANALYSIS. IT WAS STATED BY THE CUSTOMER THAT THE PRODUCT HAD BEEN DISCARDED. THUS NOT RETURNED FOR INVESTIGATION. THE DEVICE HISTORY RECORD WAS REVIEWED, AND WAS VERIFIED THAT THE DEVICE WAS MANUFACTURED IN ACCORDANCE WITH DOCUMENTED SPECIFICATION AND PROCEDURES. CONCOMITANT PRODUCTS USED DURING THE PROCEDURE: CARTO 3 SYSTEM, MODEL #: FG-5400-00M, SERIAL #: (B)(4); STOCKERT 70 SYSTEM, MODEL #: M-5463-01, SERIAL #: UNK; COOL FLOW PUMP, MODEL #: M-5491-02, SERIAL #: UNK. (B)(4).

Description of Event or Problem · 1

DURING AN ISCHEMIC VT PROCEDURE, IT WAS REPORTED WHILE ABLATING THE ABLATION CATHETER PENETRATED THE INTERVENTRICULAR SEPTUM FROM THE LEFT VENTRICLE TO THE RIGHT VENTRICLE. THE PATIENT¿S VITAL SIGNS REMAINED STABLE. ECHOCARDIOGRAPHY IDENTIFIED A VENTRICULAR SEPTAL DEFECT THAT WAS NOT SEEN PRIOR TO THE ABLATION. THE PATIENT WAS ADMITTED FOR OBSERVATION. ADDITIONAL INFORMATION WAS REQUESTED HOWEVER THERE IS NO ADDITIONAL INFORMATION AVAILABLE REGARDING THIS EVENT AT THIS TIME

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
264721 THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER CARDIAC ABLATION PERCUTANEOUS CATHETER LPB BIOSENSE WEBSTER, INC. (JUAREZ) D-1313-05-S 15832232L

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| L