VASCUTRAK PTA DILATATION CATHETER V185040S

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-15 for VASCUTRAK PTA DILATATION CATHETER V185040S manufactured by Bard Peripheral Vascular, Inc..

Event Text Entries

[177383238] For the reported event, lot number was provided, a manufacturing review will be 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 was labeled for single use.
Patient Sequence No: 1, Text Type: N, H10


[177383239] This report summarizes one malfunction. A review of the reported information indicated that model v185040s. Pta balloon dilatation catheter allegedly experienced material rupture. This report was received from a single source. This event did involve patient with no reported patient injury. Age, weight, and gender were not provided for the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2020394-2020-00279
MDR Report Key9591286
Date Received2020-01-15
Date of Report2020-04-02
Date Mfgr Received2020-03-31
Date Added to Maude2020-01-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJUDITH LUDWIG
Manufacturer Street1415 W. 3RD STREET
Manufacturer CityTEMPE AZ 85281
Manufacturer CountryUS
Manufacturer Postal85281
Manufacturer Phone4803032689
Manufacturer G1C.R. BARD, INC. (GFO)
Manufacturer Street289 BAY ROAD
Manufacturer CityQUEENSBURY NY 12804
Manufacturer CountryUS
Manufacturer Postal Code12804
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVASCUTRAK PTA DILATATION CATHETER
Generic NamePTA BALLOON DILATATION CATHETER
Product CodePNO
Date Received2020-01-15
Model NumberV185040S
Catalog NumberV185040S
Lot NumberGFDR2582
Device Availability*
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerBARD PERIPHERAL VASCULAR, INC.
Manufacturer Address1625 W 3RD ST. TEMPE AZ 85281 US 85281


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-15

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.