PACEART OPTIMA PAOPT16SUP

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-05-31 for PACEART OPTIMA PAOPT16SUP manufactured by Medtronic, Inc..

Event Text Entries

[109744042] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[109744043] It was reported that the sales representative called because the provider complained that the percent pacing displayed in patient management database application of 92% in the right atrium (ra) data field and 2% in the right ventricular (rv) data field was beyond the historical 31-32% ra pacing seen in the past. The application was working fine, and the representative was asked for additionally information for investigation; however, none was provided. The application remains in use. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2182208-2018-01009
MDR Report Key7558455
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-05-31
Date of Report2018-05-31
Date of Event2017-11-07
Date Mfgr Received2017-11-07
Date Added to Maude2018-05-31
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactANNE SCHILLING
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635052036
Manufacturer G1MEDTRONIC, INC.
Manufacturer Street8200 CORAL SEA STREET NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal Code55112
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePACEART OPTIMA
Generic NameANALYZER, PACEMAKER GENERATOR FUNCTION, INDIRECT
Product CodeKRE
Date Received2018-05-31
Model NumberPAOPT16SUP
Catalog NumberPAOPT16SUP
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC, INC.
Manufacturer Address8200 CORAL SEA STREET NE MOUNDS VIEW MN 55112 US 55112


Patients

Patient NumberTreatmentOutcomeDate
10 2018-05-31

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