PACEART OPTIMA POS12D15

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-19 for PACEART OPTIMA POS12D15 manufactured by Medtronic, Inc..

Event Text Entries

[31755265] The information submitted reflects all relevant data received. If additional relevant information is received, a supplemental report will be submitted. (b)(4)
Patient Sequence No: 1, Text Type: N, H10


[31755266] It was reported that a different encounter time and longevity value was noted in the patient management database application when compared to the information on the remote monitor database. The information was updated in the patient management database application and further investigation is being conducted to resolve the issue. The patient management database application remains in use. No patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2182208-2015-03867
MDR Report Key5237552
Date Received2015-11-19
Date of Report2015-10-26
Date of Event2015-10-25
Date Mfgr Received2015-10-26
Date Added to Maude2015-11-19
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 ContactANNE SCHILLING
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635052036
Manufacturer G1MEDTRONIC CARDIAC RHYTHM HEART FAILURE
Manufacturer Street8200 CORAL SEA ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal Code55112
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NamePACEART OPTIMA
Generic NameANALYZER, PACEMAKER GENERATOR FUNCTION, INDIRECT
Product CodeKRE
Date Received2015-11-19
Model NumberPOS12D15
Catalog NumberPOS12D15
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 2015-11-19

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