JAMSHIDI NEEDLE BONE MARROW DJ4011X

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-10-30 for JAMSHIDI NEEDLE BONE MARROW DJ4011X manufactured by Carefusion, Inc.

Event Text Entries

[126550630] (b)(4) upon completion of carefusions investigation a follow up submission will be completed.
Patient Sequence No: 1, Text Type: N, H10


[126550631] Upon inspection of our qc personnel and placement of regulatory label to each items, 5 cases of (b)(4) contain items with defective seal.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9680904-2018-00026
MDR Report Key8019340
Date Received2018-10-30
Date of Report2018-11-20
Date of Event2018-10-09
Date Mfgr Received2018-10-09
Device Manufacturer Date2018-03-14
Date Added to Maude2018-10-30
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 G1CAREFUSION, INC
Manufacturer StreetZONA FRANCA LAS AMERICAS
Manufacturer CitySANTO DOMINGO
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameJAMSHIDI NEEDLE BONE MARROW
Generic NameBIOPSY NEEDLES & TRAYS
Product CodeFSH
Date Received2018-10-30
Catalog NumberDJ4011X
Lot Number0001220841
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 2018-10-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.