FDA Adverse Event Injury Summary report: N

CATHETER, ELECTRODE RECORDING

MDR report key: 4130202 · Received September 30, 2014

Report

Report Number
2029046-2014-00345
Event Type
Injury
Date Received
September 30, 2014
Date of Event
August 5, 2008
Report Date
July 23, 2014
Manufacturer
BIOSENSE WEBSTER, INC (IRWINDALE)
Product Code
DRF
PMA / PMN Number
P030031
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

BIOSENSE WEBSTER REVIEWED "RANDOMIZED TRIAL COMPARING ROBOTIC TO MANUAL ABLATION FOR ATRIAL FIBRILLATION, HEART RHYTHM" ARTICLE AND UPON FOLLOWING UP WITH THE CUSTOMER, BWI RECEIVED ADDITIONAL INFORMATION ON (B)(4) 2014. THIS COMPLAINT IS BEING OPENED FOR THE PROCEDURE CONDUCTED ON (B)(6) 2008. THE PATIENT SUFFERED FROM RETROPERITONEAL BLEEDING. HOWEVER IT'S UNKNOWN THE PATIENT UNDERWENT ADDITIONAL SURGERY. MODEL AND CATALOG NUMBER ARE NOT AVAILABLE, BUT THE SUSPECTED DEVICE IS THE CELSIUS THERMOCOOL CATHETER. PER A REPORT IN THE JOURNAL OF HEART RHYTHM, A SINGLE-CENTER RANDOMIZED STUDY WAS CONDUCTED ON 157 PATIENTS, BY (B)(6) OF (B)(6)'S HOSPITAL, TO ASSESS THE IMPACT OF REMOTE ROBOTIC NAVIGATION ON ONE YEAR SINGLE-PROCEDURE SUCCESS RATES. FROM THE REPORT THERE WERE 13 (THIRTEEN) PATIENTS WITH SERIOUS ADVERSE EVENTS (THESE EVENTS WILL BE REPORTED SEPARATELY): PATIENT # 1 ((B)(6)): TRANSIENT ISCHEMIC ATTACK /PERICARDIAL EFFUSION/LOWER RESPIRATORY TRACT INFECTION. PATIENT # 2 ((B)(6)): CEREBROVASCULAR ACCIDENT/DEATH; PATIENT #3 ((B)(6)): RETROPERITONEAL BLEED; PATIENT #4 ((B)(6)): RETROPERITONEAL BLEED; PATIENT #5 ((B)(6)):MAJOR PULMONARY VEIN STENOSIS; PATIENT #7 ((B)(6)): LOWER RESPIRATORY TRACT INFECTION; PATIENT #8 ((B)(6)): TAMPONADE; PATIENT #10 ((B)(6)): MINOR PULMONARY VEIN STENOSIS; PATIENT #16 ((B)(6)): LOWER RESPIRATORY TRACT INFECTION; PATIENT #20 ((B)(6)): PERICARDIAL EFFUSION/ LOWER RESPIRATORY TRACT INFECTION. PER THE ARTICLE, OTHER NON-SERIOUS AE¿S WERE ALSO REPORTED: PERICARDIAL EFFUSION; HEMATOMA; PULMONARY VEIN STENOSIS. THESE EVENTS ARE NOT KNOWN TO HAVE REQUIRED INTERVENTION/TREATMENT NOR EXTENDED HOSPITALIZATION STAY. THERE IS A DEATH EVENT AND NO BWI DEVICE MALFUNCTIONS REPORTED IN THE PUBLICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
607431 CATHETER, ELECTRODE RECORDING DRF BIOSENSE WEBSTER, INC (IRWINDALE) CELSIUS THERMO TC UNKNOWN_CELSIUS THERMO TC

Patients

Seq Age Sex Outcome Treatment
1 78 YR Other