AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM 720342

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2013-02-11 for AXXENT ELECTRONIC BRACHYTHERAPY SYSTEM 720342 manufactured by Xoft.

Event Text Entries

[3332962] Balloon applicator burst while inside pt, necessitating replacement, so treatment could be delivered. Pt was not injured.
Patient Sequence No: 1, Text Type: D, B5


[10459752] Eval summary: mfg defect was confirmed and corrective action has been initiated.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3005594788-2013-00001
MDR Report Key2961670
Report Source05
Date Received2013-02-11
Date of Report2013-02-11
Date of Event2013-01-12
Date Mfgr Received2013-01-12
Device Manufacturer Date2012-09-01
Date Added to Maude2013-04-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHYSICIAN ASSISTANT
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactBONNIE MCINERNEY
Manufacturer Street101 NICHOLSON LANE
Manufacturer CitySAN JOSE CA 95134
Manufacturer CountryUS
Manufacturer Postal95134
Manufacturer Phone4084931541
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAXXENT ELECTRONIC BRACHYTHERAPY SYSTEM
Generic NameBALLOON APPLICATOR
Product CodeJAD
Date Received2013-02-11
Returned To Mfg2013-01-24
Model Number720342
Catalog Number720342
Lot Number820714
Device Expiration Date2014-09-30
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerXOFT
Manufacturer AddressSAN JOSE CA 95134 US 95134


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2013-02-11

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