MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. CARBOFLO VASCULAR GRAFT; EPTFE VASCULAR GRAFT

Model Number	40S06C
Medical Device Problem Code	Leak/Splash (1354)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
For the reported event, lot number was provided, and lot history review.The sample was not returned for evaluation and photo was provided.The company is still investigating the issue at this time.The device was labeled for single use.
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model 40s06c.Eptfe vascular graft allegedly experienced a leak.This report was received from a single source.This event did involve patient with no reported patient injury.The patients age, weight and gender were not provided.
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model 40s06c eptfe vascular graft allegedly experienced a leak.This report was received from a single source.This event did involve patient with no reported patient injury.The patients age, weight and gender were not provided.
Additional Manufacturer Narrative
H10: the lot number for the malfunction was provided and a lot history review was performed.The device has not been returned for evaluation, however, one photo was provided.After photo review, the investigation is inconclusive for a leak.Based upon the available information, a definitive root cause is unknown.The device is labeled for single use.Section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.

• Brand Name: CARBOFLO VASCULAR GRAFT
• Common Device Name: EPTFE VASCULAR GRAFT
• Manufacturer (Section D): BARD PERIPHERAL VASCULAR, INC.; 1625 w 3rd st.; tempe AZ 85281
• MDR Report Key: 9193019
• Report Number: 2020394-2019-03943
• Device Sequence Number: 19302420
• Product Code: DSY
• UDI-Device Identifier: 00801741020797
• UDI-Public: (01)00801741020797
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/02/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: No Information
• Device Model Number: 40S06C
• Device Catalogue Number: 40S06C
• Device Lot Number: VTBV0859
• Initial Date Received by Manufacturer: 09/30/2019
• Supplement Date Received by Manufacturer: 03/31/2020
• Initial Report FDA Received Date: 10/15/2019
• Supplement Report FDA Received Date: 04/02/2020
• Patient Sequence Number: 1