JAMSHIDI BONE MARROW BIOPSY DJ4011X

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-12-19 for JAMSHIDI BONE MARROW BIOPSY DJ4011X manufactured by Carefusion, Inc.

Event Text Entries

[95815102] (b)(4). A follow up submission will be done upon completion of carefusion's investigation or additional information becomes available.
Patient Sequence No: 1, Text Type: N, H10


[95815103] ?during incoming visual inspection at bd (b)(4)- (7 out of 980 ) packages were found to be unsealed, therefore sterility compromised .?
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9680904-2017-00230
MDR Report Key7129773
Date Received2017-12-19
Date of Report2018-02-08
Date of Event2017-11-24
Date Mfgr Received2017-11-24
Date Added to Maude2017-12-19
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 ANNA WEHRHEIM
Manufacturer Street75 NORTH FAIRWAY DRIVE
Manufacturer CityVERNON HILLS IL 60061
Manufacturer CountryUS
Manufacturer Postal60061
Manufacturer G1CAREFUSION, INC
Manufacturer StreetZONA FRANCA LAS AMERICAS
Manufacturer CitySANTO DOMINGO
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameJAMSHIDI BONE MARROW BIOPSY
Generic NameBIOPSY NEEDLE
Product CodeFSH
Date Received2017-12-19
Catalog NumberDJ4011X
Lot Number0001071107
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION, INC
Manufacturer AddressZONA FRANCA LAS AMERICAS SANTO DOMINGO


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-12-19

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