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

Model Number	ATG80124
Medical Device Problem Codes	Material Frayed (1262); Retraction Problem (1536); Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The lot number for the malfunction was provided; therefore, a lot history review is currently being performed.The device was returned for evaluation.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 atg80124 pta balloon dilatation catheter allegedly experienced detachment, retraction issue and frayed material.This report was received from one source.This malfunction involved one patient with no patient consequences.The device was used in a male patient.Age and weight of the patient was not provided.
Additional Manufacturer Narrative
As the lot number for the device was provided, a lot history review was performed.The sample was returned to the manufacturer for inspection/evaluation.Therefore the investigation is unconfirmed for frayed material and detachment; however it is inconclusive for retraction issue.Based on the available information, the definitive root cause for this event is unknown.The device is labeled for single use.(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 atg80124 pta balloon dilatation catheter allegedly experienced detachment, retraction issue and frayed material.This report was received from one source.This malfunction involved one patient with no patient consequences.The device was used in a male patient.Age and weight of the patient was not provided.

• Brand Name: ATLAS GOLD 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: 10300300
• Report Number: 2020394-2020-04676
• Device Sequence Number: 16261157
• Product Code: DQY
• UDI-Device Identifier: 00801741060694
• UDI-Public: (01)00801741060694
• 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): 10/15/2020

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: ATG80124
• Device Catalogue Number: ATG80124
• Device Lot Number: 93WD0102
• Initial Date Received by Manufacturer: 06/30/2020
• Supplement Date Received by Manufacturer: 09/30/2020
• Initial Report FDA Received Date: 07/21/2020
• Supplement Report FDA Received Date: 10/15/2020
• Patient Sequence Number: 1