MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. FLUENCY PLUS ENDOVASCULAR STENT GRAFT

Model Number	FEM14100
Medical Device Problem Codes	Positioning Failure (1158); Misfire (2532)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model fem14100 endovascular stent graft allegedly experienced positioning failure.This information was received from one source.The event involved a patient with no known impact to the patient.The age, weight and gender of the patient were not provided.
Additional Manufacturer Narrative
H10: as the lot number for the device was provided, a lot history review was performed.The device has been returned to the manufacturer for evaluation.The investigation is confirmed for positioning failure and misfire.A definitive root cause for the reported event could not be determined.The device is labeled for single use.H11: 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.
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model fem14100 endovascular stent graft allegedly experienced positioning failure.This information was received from one source.The event involved a patient with no known impact to the patient.The age, weight and gender of the patient were not provided.

• Brand Name: FLUENCY PLUS ENDOVASCULAR STENT GRAFT
• Common Device Name: ENDOVASCULAR STENT GRAFT
• Manufacturer (Section D): BARD PERIPHERAL VASCULAR, INC.; 1625 w 3rd st.; tempe AZ 85281
• MDR Report Key: 10276625
• Report Number: 2020394-2020-04463
• Device Sequence Number: 14084885
• Product Code: PFV
• UDI-Device Identifier: 04049519008714
• UDI-Public: (01)04049519008714
• 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): 10/12/2020

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: FEM14100
• Device Catalogue Number: FEM14100
• Device Lot Number: ANDX1922
• Initial Date Received by Manufacturer: 06/30/2020
• Supplement Date Received by Manufacturer: 09/30/2020
• Initial Report FDA Received Date: 07/15/2020
• Supplement Report FDA Received Date: 10/12/2020
• Patient Sequence Number: 1