MAUDE Adverse Event Report: BARD PERIPHERAL VASCULAR, INC. ULTRAVERSE 035 PTA CATHETER; PTA BALLOON DILATATION CATHETER

Model Number	U354044
Medical Device Problem Code	Material Rupture (1546)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The lot number was provided and a lot history review will be performed.The sample was returned for evaluation.The company is still investigating the issue at this time.The device was labeled for single use.
Event or Problem Description
This report summarizes a single malfunction.A review of the reported information indicated that model u354044, pta balloon dilatation catheter, allegedly experienced material rupture.This information was received from a single source.This malfunction involved a patient with no consequences.The patient's age, weight, and gender were not provided.
Additional Manufacturer Narrative
H10: the reported malfunction was reassessed for reportability and determine to be no longer reportable.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 a single malfunction.A review of the reported information indicated that model u354044, pta balloon dilatation catheter, allegedly experienced material rupture.This information was recieved from a single source.This malfunction involved a patient with no consequences.The paient's age, weight, and gender were not provided.

• Brand Name: ULTRAVERSE 035 PTA 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: 9593785
• Report Number: 2020394-2020-00387
• Device Sequence Number: 328052
• Product Code: LIT
• UDI-Device Identifier: 00801741091896
• UDI-Public: (01)00801741091896
• 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): 03/30/2020

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: U354044
• Device Catalogue Number: U354044
• Device Lot Number: CMDQ0499
• Initial Date Received by Manufacturer: 12/31/2019
• Supplement Date Received by Manufacturer: 03/30/2020
• Initial Report FDA Received Date: 01/15/2020
• Supplement Report FDA Received Date: 04/01/2020
• Patient Sequence Number: 1