ILLINOIS NEEDLE BONE MARROW 15G ADJ LE DIN1515X

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,other report with the FDA on 2020-01-31 for ILLINOIS NEEDLE BONE MARROW 15G ADJ LE DIN1515X manufactured by Carefusion, Inc.

MAUDE Entry Details

Report Number9680904-2020-00003
MDR Report Key9654553
Report SourceDISTRIBUTOR,OTHER
Date Received2020-01-31
Date of Report2020-03-27
Date of Event2020-01-06
Date Mfgr Received2020-01-06
Date Added to Maude2020-01-31
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 ANNA WEHRHEIM
Manufacturer Street75 N. FAIRVIEW DRIVE
Manufacturer CityVERNON HILLS IL 60061
Manufacturer CountryUS
Manufacturer Postal60061
Manufacturer Phone8015652341
Manufacturer G1CAREFUSION, INC
Manufacturer StreetZONA FRANCA LAS AMERICAS
Manufacturer CitySANTO DOMINGO
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameILLINOIS NEEDLE BONE MARROW 15G ADJ LE
Generic NameTRAY, SURGICAL, NEEDLE
Product CodeFSH
Date Received2020-01-31
Catalog NumberDIN1515X
Lot Number0001314966
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION, INC
Manufacturer AddressZONA FRANCA LAS AMERICAS SANTO DOMINGO


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-01-31

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