DRAGONFLY? OPTIS? KIT BOX IMAGING CATHETER C408646

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2017-10-20 for DRAGONFLY? OPTIS? KIT BOX IMAGING CATHETER C408646 manufactured by St. Jude Medical.

Event Text Entries

[89860492] An event of cardiac ischemia was reported. The results of the investigation are inconclusive since the device was not returned for analysis. Based on the information received, the cause of the reported incident could not be conclusively determined. The dragonfly optis instructions for use states coronary artery spasm may occur as a consequence of intravascular imaging
Patient Sequence No: 1, Text Type: N, H10


[89860493] After the dragonfly optis catheter was advanced and just prior to a pullback, the vessel closed down. It was suspected the issue was caused by a vessel spasm. The patient was treated with nitro. The stenting procedure was completed without oct.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3009600098-2017-00005
MDR Report Key6965861
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2017-10-20
Date of Report2017-10-20
Date Mfgr Received2017-10-05
Date Added to Maude2017-10-20
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 ContactDENISE JOHNSON
Manufacturer Street5050 NATHAN LANE NORTH
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1ST. JUDE MEDICAL
Manufacturer Street4 ROBBINS DRIVE
Manufacturer CityWESTFORD MA 01886
Manufacturer CountryUS
Manufacturer Postal Code01886
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDRAGONFLY? OPTIS? KIT BOX IMAGING CATHETER
Generic NameDRAGONFLY OPTIS CATHETER
Product CodeORD
Date Received2017-10-20
Model NumberC408646
Catalog NumberC408646
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL
Manufacturer Address4 ROBBINS DRIVE WESTFORD MA 01886 US 01886


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-10-20

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