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

Model Number	CQ5054
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 for the reported malfunction; therefore, a lot history review is currently being performed.The sample was not returned to the manufacturer for inspection/evaluation.Therefore, the investigation of the reported event is inconclusive.Based upon the available information, the definitive root cause for this event is unknown.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 cq5054 conquest pta dilatation catheter allegedly experienced material rupture.This information was received from one source.Of the one material rupture malfunction, one patient was involved with no patient consequence or impact.Patient age, weight, and gender was not provided.
Additional Manufacturer Narrative
H10: the reported information has been reviewed and it has been determined that this malfunction is no longer reportable.The lot number was provided for the reported malfunction; therefore, a lot history review is currently being performed.The sample was returned to the manufacturer for inspection/evaluation.The evaluation identified a pinhole rupture.Based upon the available information, the definitive root cause for this event is unknown.The device is labeled for single use.H10: g4.H11: h6 (method, results, conclusion).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 cq5054 conquest pta dilatation catheter allegedly experienced material rupture.This information was received from one source.Of the one material rupture malfunction, one patient was involved with no patient consequence or impact.Patient age, weight, and gender was not provided.

• Brand Name: CONQUEST PTA DILATATION CATHETR
• Common Device Name: PTA BALLOON DILATATION CATHETER
• Manufacturer (Section D): BARD PERIPHERAL VASCULAR, INC.; 1625 w 3rd st.; tempe AZ 85281
• MDR Report Key: 9593430
• Report Number: 2020394-2020-00353
• Device Sequence Number: 374648
• Product Code: DQY
• UDI-Device Identifier: 00801741062803
• UDI-Public: (01)00801741062803
• 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: CQ5054
• Device Catalogue Number: CQ5054
• Device Lot Number: REDS1491
• Initial Date Received by Manufacturer: 12/31/2019
• Supplement Date Received by Manufacturer: 03/25/2020
• Initial Report FDA Received Date: 01/15/2020
• Supplement Report FDA Received Date: 04/02/2020
• Patient Sequence Number: 1