BD ADAMS? COMPACT II CENTRIFUGE 421417

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 2019-11-25 for BD ADAMS? COMPACT II CENTRIFUGE 421417 manufactured by Becton, Dickinson & Co..

MAUDE Entry Details

Report Number1119779-2019-00118
MDR Report Key9369913
Report SourceOTHER,USER FACILITY
Date Received2019-11-25
Date of Report2020-03-23
Date of Event2019-09-01
Date Mfgr Received2019-11-01
Date Added to Maude2019-11-25
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 & CO.
Manufacturer Street7 LOVETON CIRCLE
Manufacturer CitySPARKS MD 21152
Manufacturer CountryUS
Manufacturer Postal Code21152
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBD ADAMS? COMPACT II CENTRIFUGE
Generic NameGENERAL PURPOSE LABORATORY EQUIPMENT
Product CodeLXG
Date Received2019-11-25
Catalog Number421417
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON & CO.
Manufacturer Address7 LOVETON CIRCLE SPARKS MD 21152 US 21152


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-25

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