BD VACUTAINER BULK GEL 368586

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-21 for BD VACUTAINER BULK GEL 368586 manufactured by Becton, Dickinson & Co., (bd).

MAUDE Entry Details

Report Number1024879-2019-01485
MDR Report Key8914848
Date Received2019-08-21
Date of Report2019-09-16
Date of Event2019-08-05
Date Mfgr Received2019-08-05
Device Manufacturer Date2019-04-18
Date Added to Maude2019-08-21
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., (BD)
Manufacturer Street1575 AIRPORT ROAD
Manufacturer CitySUMTER SC 29153
Manufacturer CountryUS
Manufacturer Postal Code29153
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBD VACUTAINER BULK GEL
Generic NameCPT GEL
Product CodeJCF
Date Received2019-08-21
Catalog Number368586
Lot Number9108673
Device Expiration Date2019-07-26
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBECTON, DICKINSON & CO., (BD)
Manufacturer Address1575 AIRPORT ROAD SUMTER SC 29153 US 29153


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-08-21

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