BD BLUNT FILL NEEDLE WITH FILTER 305211

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,user facility report with the FDA on 2020-01-09 for BD BLUNT FILL NEEDLE WITH FILTER 305211 manufactured by Becton Dickinson And Company.

MAUDE Entry Details

Report Number1911916-2019-01381
MDR Report Key9570328
Report SourceOTHER,USER FACILITY
Date Received2020-01-09
Date of Report2019-12-20
Date of Event2019-12-06
Date Mfgr Received2019-12-17
Device Manufacturer Date2018-02-16
Date Added to Maude2020-01-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactBDX BRETT WILKO
Manufacturer Street9450 SOUTH STATE STREET
Manufacturer CitySANDY UT 84070
Manufacturer CountryUS
Manufacturer Postal84070
Manufacturer Phone8015652341
Manufacturer G1BECTON DICKINSON AND COMPANY
Manufacturer Street2153 12TH AVENUE
Manufacturer CityCOLUMBUS NE 68601
Manufacturer CountryUS
Manufacturer Postal Code68601
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD BLUNT FILL NEEDLE WITH FILTER
Generic NameNEEDLE FILTER BLUNT FILL 18X1-1/2
Product CodeGAA
Date Received2020-01-09
Catalog Number305211
Lot Number8047736
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON AND COMPANY
Manufacturer Address2153 12TH AVENUE COLUMBUS NE 68601 US 68601


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-09

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