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 from a health professional,other report with the FDA on 2016-02-01 for BLOOD COLLECTION DEVICE W/MALE LUER MBC6010 manufactured by Carefusion.

Event Text Entries

[37240802] The customer's reported complaint could not be confirmed because the set has been discarded by the customer and will not be returned. The root cause of this failure could not be identified.
Patient Sequence No: 1, Text Type: N, H10


[37240803] Customer reported that the blood continued to flow out of the vacutainer while changing tubes. There was no harm to the clinician or patient as a result of the event, and no further information or details are available.
Patient Sequence No: 1, Text Type: D, B5


[45245304]
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9616066-2016-00185
MDR Report Key5402108
Report SourceHEALTH PROFESSIONAL,OTHER
Date Received2016-02-01
Date of Report2016-01-18
Date Mfgr Received2016-04-22
Date Added to Maude2016-02-01
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 Report3

Device Details

Brand NameBLOOD COLLECTION DEVICE W/MALE LUER
Generic NameSYSTEM, BLOOD COLLECTION, VACUUM-ASSISTED, MANUAL
Product CodeKST
Date Received2016-02-01
Model NumberMBC6010
Catalog NumberMBC6010
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
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 2016-02-01

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