THERMOCOOL® SF NAV BI-DIRECTIONAL CATHETER
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
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).
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 |