BD POSIFLUSH SYRINGE 10ML SALINE XS 306572

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 2020-02-17 for BD POSIFLUSH SYRINGE 10ML SALINE XS 306572 manufactured by Becton, Dickinson And Co..

MAUDE Entry Details

Report Number9616657-2020-00027
MDR Report Key9718038
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2020-02-17
Date of Report2020-01-28
Date of Event2020-01-28
Date Mfgr Received2020-01-28
Device Manufacturer Date2019-06-12
Date Added to Maude2020-02-17
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 CO.
Manufacturer StreetDONORE ROAD
Manufacturer CityDROGHEDA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD POSIFLUSH SYRINGE 10ML SALINE XS
Generic NameSALINE FLUSH SYRINGE
Product CodeNGT
Date Received2020-02-17
Catalog Number306572
Lot Number9163585
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON AND CO.
Manufacturer AddressDONORE ROAD DROGHEDA


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-02-17

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.