GHIATAS BEADED BREAST LOCALIZATION WIRE 47920

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 2018-10-29 for GHIATAS BEADED BREAST LOCALIZATION WIRE 47920 manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[125445938] No medical records and no medical images were provided to the manufacturer. The lot number for the device was provided. The device history records are currently under review. The device has been returned for evaluation. The investigation of the reported event is currently underway. (expiry date: nov2020).
Patient Sequence No: 1, Text Type: N, H10


[125445939] It was reported that upon opening the package, the device allegedly was not clean. It was further reported that the procedure was performed with another device. There was no patient contact.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2018-01949
MDR Report Key8016792
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-10-29
Date of Report2018-10-29
Date of Event2018-09-30
Date Mfgr Received2018-10-05
Device Manufacturer Date2018-01-12
Date Added to Maude2018-10-29
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 ContactJUDITH LUDWIG
Manufacturer Street1625 W 3RD ST.
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1BARD REYNOSA S.A. DE C.V.
Manufacturer StreetBLVD MONTEBELLO #1 PARQUE INDUSTRIAL COLONIAL
Manufacturer CityREYNOSA TAMAULIPAS 88780
Manufacturer CountryMX
Manufacturer Postal Code88780
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameGHIATAS BEADED BREAST LOCALIZATION WIRE
Generic NameLOCALIZATION WIRE
Product CodeGDF
Date Received2018-10-29
Returned To Mfg2018-10-25
Model Number47920
Catalog Number47920
Lot NumberREBY2181
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2018-10-29

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