KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE DKBL-20-5.0-A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2018-04-23 for KOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE DKBL-20-5.0-A manufactured by Cook Inc.

Event Text Entries

[106632912] Pma/510 (k): exempt. (b)(4). This report includes information known at this time. A follow up report will be submitted should additional relevant information become available.
Patient Sequence No: 1, Text Type: N, H10


[106632913] The customer reported that the external wire of kopans modified breast lesion localization needle snapped off. The device did not remain in the patient's body. It was reported that the patient did not require any additional procedures and did not experience any adverse events.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1820334-2018-01142
MDR Report Key7450454
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2018-04-23
Date of Report2018-05-16
Date Mfgr Received2018-05-14
Date Added to Maude2018-04-23
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 ContactMR. LARRY POOL
Manufacturer Street750 DANIELS WAY
Manufacturer CityBLOOMINGTON IN 47404
Manufacturer CountryUS
Manufacturer Postal47404
Manufacturer Phone8123392235
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKOPANS MODIFIED BREAST LESION LOCALIZATION NEEDLE
Generic NameMIJ NEEDLE, TUMOR LOCALIZATION
Product CodeMIJ
Date Received2018-04-23
Catalog NumberDKBL-20-5.0-A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOOK INC
Manufacturer Address750 DANIELS WAY BLOOMINGTON IN 47404 US 47404


Patients

Patient NumberTreatmentOutcomeDate
10 2018-04-23

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