CARBOFLO VASCULAR GRAFT 10S06TWC

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-14 for CARBOFLO VASCULAR GRAFT 10S06TWC manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[177377088] The lot number was provided and a lot history review was performed. The sample was not returned to bd for evaluation. Therefore, the investigation of the reported malfunction is inconclusive. Based upon the information provided, the definitive root cause is unknown. The device was labeled for single use.
Patient Sequence No: 1, Text Type: N, H10


[177377089] This report summarizes one malfunction. A review of the reported information indicated that model 10s06twc eptfe vascular graft allegedly experienced a material tear. This information was received from one source. This malfunction did involve a patient with no reported patient injury. The patient's age, weight, and gender were not provided.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2020-00223
MDR Report Key9587241
Date Received2020-01-14
Date of Report2020-01-14
Date Mfgr Received2019-12-31
Date Added to Maude2020-01-14
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 ContactJUDITH LUDWIG
Manufacturer Street1415 W. 3RD STREET
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 CodeDSY
Date Received2020-01-14
Model Number10S06TWC
Catalog Number10S06TWC
Lot NumberVTCZ0262
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-14

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