DYNAMIC XT 86706

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-24 for DYNAMIC XT 86706 manufactured by Boston Scientific Corporation.

Event Text Entries

[184740561] It was indicated that the device will not be returned for evaluation. If there is any further relevant information obtained, a supplemental medwatch will be filed.
Patient Sequence No: 1, Text Type: N, H10


[184740562] It was reported that the patient experienced a cardiac tamponade and perforation. During a redo pulmonary vein isolation (pvi) ablation procedure, with an intellamap orion high resolution mapping catheter, an intellanav mifi open-irrigated ablation catheter, a dynamic xt electrode catheter and two non-boston scientific 8. 5f sheaths, a perforation of left atrium near the base of the appendix occurred. Aspiration was not sufficient, so surgical intervention was required. The perforation closed and the patient was stabilized. It was suspected the intellanav mifi open-irrigated ablation catheter caused the tamponade as the puncture was found to be at the base of that appendage. Since the issue was noticed at the very end of the procedure, after cardioversion, it was considered less likely this was caused by the transeptal puncture. It was not known if it was due to hard pushing or too much ablation. The physician didn't note any resistance maneuvering any of catheters. All of the devices used were disposed of.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-03774
MDR Report Key9873569
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-24
Date of Report2020-03-24
Date of Event2020-03-11
Date Mfgr Received2020-03-11
Date Added to Maude2020-03-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTIMOTHY DEGROOT
Manufacturer Street4100 HAMLINE AVENUE NORTH DC A330
Manufacturer CitySAINT PAUL MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone6515826168
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer Street302 PARKWAY, GLOBAL PARK
Manufacturer CityLA AURORA - HEREDIA
Manufacturer CountryCS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDYNAMIC XT
Generic NameCATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Product CodeDRF
Date Received2020-03-24
Model Number86706
Catalog Number86706
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
191. Required No Informationntervention 2020-03-24

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