PACEART OPTIMA PAOPT17SUP

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-10-15 for PACEART OPTIMA PAOPT17SUP manufactured by Medtronic, Inc..

Event Text Entries

[123805003] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[123805004] It was reported that the caller complained that after the hl-7 configuration in the patient management database application that the manufacturer was moving the local time zone was changing the device implant date to an earlier date. After turning on the additional outbound action list customization to convert to the local time, the caller reported that the implant dates displayed unwanted feature times from the previous day. The issue was escalated to the developer. It was found that the send date only would undone by converting; therefore, omitting the conversion and adding in not equal if clauses. The application remains in us. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2182208-2018-01875
MDR Report Key7967498
Report SourceHEALTH PROFESSIONAL
Date Received2018-10-15
Date of Report2018-10-15
Date of Event2018-09-19
Date Mfgr Received2018-09-19
Date Added to Maude2018-10-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 Received2018-10-15
Model NumberPAOPT17SUP
Catalog NumberPAOPT17SUP
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 2018-10-15

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