AMPLATZER SEPTAL OCCLUDER 9-ASD-010

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 2020-03-20 for AMPLATZER SEPTAL OCCLUDER 9-ASD-010 manufactured by Aga Medical Corporation.

Event Text Entries

[184307368] Further information regarding this event has been requested. Investigation results will be provided in a subsequent submission when received.
Patient Sequence No: 1, Text Type: N, H10


[184307369] A 10mm amplatzer septal occluder (9-asd-010 lot #7053280) was chosen for asd closure procedure. Upon deploying the device the left atrial disk was "cobra" misaligned. The user tried several different techniques to get the device to deploy but he was unsuccessful. He pulled a second 10mm amplatzer septal occluder (9-asd-010 lot #7097787) and the device closed the defect.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2135147-2020-00116
MDR Report Key9860648
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-20
Date of Report2020-03-20
Date of Event2020-03-05
Date Mfgr Received2020-03-05
Device Manufacturer Date2019-06-19
Date Added to Maude2020-03-20
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 ContactPAMELA YIP
Manufacturer Street5050 NATHAN LANE N
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1AGA MEDICAL CORPORATION
Manufacturer Street5050 NATHAN LANE NORTH
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal Code55442
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMPLATZER SEPTAL OCCLUDER
Generic NameTRANSCATHETER SEPTAL OCCLUDER
Product CodeMLV
Date Received2020-03-20
Model Number9-ASD-010
Catalog Number9-ASD-010
Lot Number7053280
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerAGA MEDICAL CORPORATION
Manufacturer Address5050 NATHAN LANE NORTH PLYMOUTH MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-20

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