MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. VACCESS PTA DILATATION CATHETER; PTA BALLOON DILATATION CATHETER

Model Number	VA8086
Medical Device Problem Code	Retraction Problem (1536)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device is return for the one complaint.The company is still investigating the issue at this time.The device is labeled for single use.
Event or Problem Description
This report summarizes one malfunction.A review of the reported information indicated that model va8086.Pta balloon dilatation catheter allegedly experienced retraction problem.This report was received from a single source.This event did involve patient with no reported patient injury.The patient is (b)(6) years of age, the gender is male, and the weight is (b)(6) kgs.
Additional Manufacturer Narrative
The device is return to bd for evaluation the investigation is confirmed for a retraction issue, as the device was returned stuck in the sheath with bunching and buckling noted to the sheath.Based on the information provided, the definitive root cause is unknown.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 va8086.Pta balloon dilatation catheter allegedly experienced retraction problem.This report was received from a single source.This malfunction did involve patient with no reported patient injury.The patient is 74 years of age, the gender is male, and the weight is 155 kgs.

• Brand Name: VACCESS PTA DILATATION CATHETER
• Common Device Name: PTA BALLOON DILATATION CATHETER
• Manufacturer (Section D): BARD PERIPHERAL VASCULAR, INC.; 1625 w 3rd st.; tempe AZ 85281
• MDR Report Key: 8812540
• Report Number: 2020394-2019-01671
• Device Sequence Number: 2536713
• Product Code: DQY
• UDI-Device Identifier: 00801741121340
• UDI-Public: (01)00801741121340
• 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): 10/17/2019

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: VA8086
• Device Catalogue Number: VA8086
• Device Lot Number: 93QD0013
• Initial Date Received by Manufacturer: 06/30/2019
• Supplement Date Received by Manufacturer: 09/30/2019
• Initial Report FDA Received Date: 07/22/2019
• Supplement Report FDA Received Date: 10/17/2019
• Patient Sequence Number: 1