BLOOD COLLECTION DEVICE MBC6000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2015-10-30 for BLOOD COLLECTION DEVICE MBC6000 manufactured by Carefusion.

Event Text Entries

[29950270] No product will be returned per customer. The customer complaint could not be confirmed because the product was discarded and not returned for failure investigation. The root cause of this failure was not identified.
Patient Sequence No: 1, Text Type: N, H10


[29950271] The customer reported multiple occurrences of the rubber sheath covering the needle would become lodged inside of the blood culture vial when obtaining samples using the blood collection device. No patient harm reported.
Patient Sequence No: 1, Text Type: D, B5


[45247317] Correction on initial report.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number9616066-2015-01376
MDR Report Key5191553
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2015-10-30
Date of Report2015-10-16
Date Mfgr Received2016-04-22
Device Manufacturer Date2015-04-14
Date Added to Maude2015-10-30
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SYLVIA VENTURA
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
Generic NameBLOOD COLLECTION
Product CodeKST
Date Received2015-10-30
Model NumberMBC6000
Catalog NumberMBC6000
Lot Number301150414
Device Expiration Date2018-04-01
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 2015-10-30

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