BARD BRACHYSTAR BRACHYTHERAPY APPLICATOR NEEDLE 918201

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-11-21 for BARD BRACHYSTAR BRACHYTHERAPY APPLICATOR NEEDLE 918201 manufactured by Bard Brachytherapy, Inc. -1424526.

Event Text Entries

[128198506] The investigation is still in progress. Once the investigation is complete a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[128198507] It was reported that the user found it difficult to insert the needle thus, another needle was used.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1018233-2018-05618
MDR Report Key8097127
Date Received2018-11-21
Date of Report2018-11-21
Date of Event2018-11-01
Date Mfgr Received2018-11-02
Date Added to Maude2018-11-21
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 ContactYONIC ANDERSON
Manufacturer Street8195 INDUSTRIAL BLVD
Manufacturer CityCOVINGTON GA 30014
Manufacturer CountryUS
Manufacturer Postal30014
Manufacturer Phone7707846100
Manufacturer G1BARD BRACHYTHERAPY, INC. -1424526
Manufacturer Street295 EAST LIES ROAD
Manufacturer CityCAROL STREAM IL 60188
Manufacturer CountryUS
Manufacturer Postal Code60188
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBARD BRACHYSTAR BRACHYTHERAPY APPLICATOR NEEDLE
Generic NameBRACHY NEEDLE
Product CodeIWJ
Date Received2018-11-21
Returned To Mfg2018-12-07
Catalog Number918201
Lot NumberUNK
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBARD BRACHYTHERAPY, INC. -1424526
Manufacturer Address295 EAST LIES ROAD CAROL STREAM IL 60188 US 60188


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-21

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