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

Model Number	U41502H15RX
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Event or Problem Description
This report summarizes two malfunctions.A review of reported information indicates that model u41502h15rx, pta balloon dilatation catheter, allegedly experienced material rupture.This information was received from multiple sources.These malfunctions involved patients with no consequences.Neither patients' age, weight, or gender was provided.

• Brand Name: ULTRAVERSE RX PTA DILATATION BALLOON 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: 9963765
• Report Number: 2020394-2020-02722
• Device Sequence Number: 2546600
• Product Code: LIT
• UDI-Device Identifier: 00801741056628
• UDI-Public: (01)00801741056628
• 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
• Report Date (Section B): 04/15/2020

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: U41502H15RX
• Device Catalogue Number: U41502H15RX
• Device Lot Number: CMCS0179, CMDQ0277
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/31/2020
• Initial Report FDA Received Date: 04/15/2020
• Patient Sequence Number: 1