MAXGUARD? BLOOD COLLECTION TUBE HOLDER MBC6000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2016-03-14 for MAXGUARD? BLOOD COLLECTION TUBE HOLDER MBC6000 manufactured by Carefusion.

Event Text Entries

[40245594] No product will be returned per customer. The customer? S complaint could not be confirmed because the product was not sequestered and will not be returned for failure investigation. The root cause of this failure was not identified.
Patient Sequence No: 1, Text Type: N, H10


[40245595] The customer reported that the rubber got stuck in the blood collection device and leaked. There is no report of any patient harm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9616066-2016-00381
MDR Report Key5498277
Report SourceDISTRIBUTOR,FOREIGN,OTHER
Date Received2016-03-14
Date of Report2016-02-23
Date of Event2016-02-17
Date Mfgr Received2016-02-23
Device Manufacturer Date2014-12-19
Date Added to Maude2016-03-14
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 NameMAXGUARD? BLOOD COLLECTION TUBE HOLDER
Generic NameSYSTEM, BLOOD COLLECTION,VACUUM-ASST
Product CodeKST
Date Received2016-03-14
Model NumberMBC6000
Catalog NumberMBC6000
Lot Number301141219
Device Expiration Date2017-12-01
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 2016-03-14

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