CARBOFLO VASCULAR GRAFT 40S06C

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2018-12-06 for CARBOFLO VASCULAR GRAFT 40S06C manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[129512240] No medical records and no medical images were provided to the manufacturer. The lot number for the device was provided. The device history records are currently under review. The return of the device is pending. The investigation is currently under way.
Patient Sequence No: 1, Text Type: N, H10


[129512241] It was reported during preparation, the graft was allegedly leaked after injecting heparin. No further information was provided. There was no reported patient contact.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2018-02167
MDR Report Key8138349
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-12-06
Date of Report2018-12-06
Date of Event2018-11-12
Date Mfgr Received2018-11-12
Date Added to Maude2018-12-06
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 ContactJUDITH LUDWIG
Manufacturer Street1625 W 3RD ST.
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1BARD PERIPHERAL VASCULAR, INC.
Manufacturer Street1625 W 3RD ST.
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal Code85281
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCARBOFLO VASCULAR GRAFT
Generic NameEPTFE VASCULAR GRAFT
Product CodeDYF
Date Received2018-12-06
Returned To Mfg2019-01-02
Model Number40S06C
Catalog Number40S06C
Lot NumberVTBW0537
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2018-12-06

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