BD SYRINGE S2 NS 20ML 309210

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2020-02-25 for BD SYRINGE S2 NS 20ML 309210 manufactured by Becton Dickinson, S.a..

MAUDE Entry Details

Report Number3002682307-2020-00064
MDR Report Key9751980
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2020-02-25
Date of Report2020-03-23
Date of Event2020-02-05
Date Mfgr Received2020-02-05
Device Manufacturer Date2019-03-12
Date Added to Maude2020-02-25
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, S.A.
Manufacturer StreetCR MEQUINENZA S/N
Manufacturer CityFRAGA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD SYRINGE S2 NS 20ML
Generic NameSALINE FLUSH
Product CodeNGT
Date Received2020-02-25
Catalog Number309210
Lot Number9071807
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECTON DICKINSON, S.A.
Manufacturer AddressCR MEQUINENZA S/N FRAGA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-25

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