BLOOD COLLECTION DEVICE W/MALE LUER MBC6010

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-03-21 for BLOOD COLLECTION DEVICE W/MALE LUER MBC6010 manufactured by Carefusion.

Event Text Entries

[139554196] Unable to determine the cause of the customer's reported complaint because the set has been discarded by the customer and will not be returned. The root cause of this failure could not be identified. Additional patient information: diagnosis; esrd.
Patient Sequence No: 1, Text Type: N, H10


[139554257] The customer reported that davita in-center staff have stated that while disconnecting the blood collection assembly with the male luer, the male luer threads are breaking off into the cannulation line. The staff are using pliers to remove the broken pieces from the line. There was no report of patient harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616066-2019-00744
MDR Report Key8441723
Date Received2019-03-21
Date of Report2019-02-28
Date Added to Maude2019-03-21
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 ContactMR. STEPHEN BILELLO
Manufacturer Street10020 PACIFIC MESA BLVD
Manufacturer CitySAN DIEGO CA 921214386
Manufacturer CountryUS
Manufacturer Postal921214386
Manufacturer Phone8586172000
Manufacturer G1CAREFUSION
Manufacturer Street10020 PACIFIC MESA BLVD
Manufacturer CitySAN DIEGO CA 921214386
Manufacturer CountryUS
Manufacturer Postal Code921214386
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameBLOOD COLLECTION DEVICE W/MALE LUER
Generic NameSYSTEM, BLOOD COLLECTION,VACUUM-ASST
Product CodeKST
Date Received2019-03-21
Model NumberMBC6010
Catalog NumberMBC6010
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION
Manufacturer Address10020 PACIFIC MESA BLVD SAN DIEGO CA 921214386 US 921214386


Patients

Patient NumberTreatmentOutcomeDate
10 2019-03-21

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