THERMODILUTION CATH KIT: 7.5 FR 5-L IPN036076 AH-05050-G

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-01-16 for THERMODILUTION CATH KIT: 7.5 FR 5-L IPN036076 AH-05050-G manufactured by Arrow International Inc..

Event Text Entries

[183923181] Qn#1900074585
Patient Sequence No: 1, Text Type: N, H10


[183923182] It was reported that "during use on the patient the physician inserted the catheter and was able to measure pressures in ra (right atrium), rv (right ventricle) and svc (superior vena cava) but was unable to reach the pulmonary artery. It was reported that a second catheter was used but the therapy was not finished. Clinical consequences: there were no report of any clinical consequence or patient complications. In the meanwhile the patient was discharged home from the hospital.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010532612-2020-00016
MDR Report Key9597299
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-01-16
Date of Report2019-12-30
Date of Event2019-12-20
Date Mfgr Received2020-02-25
Device Manufacturer Date2019-06-17
Date Added to Maude2020-01-16
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 ContactCARMEN SHERMAN
Manufacturer Street16 ELIZABETH DRIVE
Manufacturer CityCHELMSFORD MA 01824
Manufacturer CountryUS
Manufacturer Postal01824
Manufacturer Phone9782505100
Manufacturer G1ARROW INTERNATIONAL INC.
Manufacturer Street16 ELIZABETH DRIVE
Manufacturer CityCHELMSFORD MA 01824
Manufacturer CountryUS
Manufacturer Postal Code01824
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTHERMODILUTION CATH KIT: 7.5 FR 5-L
Generic NameCATHETER, FLOW DIRECTED
Product CodeDYG
Date Received2020-01-16
Returned To Mfg2020-01-22
Model NumberIPN036076
Catalog NumberAH-05050-G
Lot Number71F19E3167
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-16

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