BD SPINAL NEEDLE 27GA 3-1/2IN 408381

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2020-01-14 for BD SPINAL NEEDLE 27GA 3-1/2IN 408381 manufactured by Becton Dickinson Industrias Cirurgicas, Ltda..

MAUDE Entry Details

Report Number9610048-2019-00368
MDR Report Key9587279
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-01-14
Date of Report2020-03-26
Date of Event2019-12-11
Date Mfgr Received2019-12-27
Device Manufacturer Date2019-03-15
Date Added to Maude2020-01-14
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 INDUSTRIAS CIRURGICAS, LTDA.
Manufacturer StreetAVE. PRES.JUSCELINO KUBITSCHEK 273 FRANCISCO BERNARDINO
Manufacturer CityJUIZ DE FORA
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD SPINAL NEEDLE 27GA 3-1/2IN
Generic NameSPINAL NEEDLE
Product CodeMIA
Date Received2020-01-14
Catalog Number408381
Lot Number9058939
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.
Manufacturer AddressAVE. PRES.JUSCELINO KUBITSCHEK 273 FRANCISCO BERNARDINO JUIZ DE FORA US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-14

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