BD SERO-FUGE? 2002 CENTRIFUGE, 2 SPEED, 115V 420352

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-03-30 for BD SERO-FUGE? 2002 CENTRIFUGE, 2 SPEED, 115V 420352 manufactured by Becton, Dickinson & Co..

Event Text Entries

[104157562] A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10


[104157563] It was reported that a bd sero-fuge? 2002 centrifuge, 2 speed, 115v continued to run when the lid was open. No injury or medical intervention.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1119779-2018-00005
MDR Report Key7387318
Date Received2018-03-30
Date of Report2019-01-09
Date of Event2018-03-05
Date Mfgr Received2018-03-05
Device Manufacturer Date2018-03-05
Date Added to Maude2018-03-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 Phone8015652845
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 Report0

Device Details

Brand NameBD SERO-FUGE? 2002 CENTRIFUGE, 2 SPEED, 115V
Generic NameCENTRIFUGE
Product CodeLXG
Date Received2018-03-30
Catalog Number420352
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON & CO.
Manufacturer Address7 LOVETON CIRCLE SPARKS MD 21152 US 21152


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-03-30

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