CARDIOMEMS PATIENT ELECTRONIC SYSTEM CM1100

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 2020-03-25 for CARDIOMEMS PATIENT ELECTRONIC SYSTEM CM1100 manufactured by St. Jude Medical, Inc..

Event Text Entries

[188741285] No device analysis is available because the device was not returned. The issue was resolved through troubleshooting. The cause of the reported event remains unknown.
Patient Sequence No: 1, Text Type: N, H10


[188741286] It was reported that the patient electronic unit received an error 5 message, which indicates an issue related to temperature and barometric pressure. The issue was resolved through troubleshooting.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004936110-2020-00120
MDR Report Key9878216
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-25
Date of Report2020-03-25
Date of Event2020-03-09
Date Mfgr Received2020-03-09
Device Manufacturer Date2018-05-11
Date Added to Maude2020-03-25
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 ContactSTEPHANIE O' SULLIVAN
Manufacturer Street5050 NATHAN LANE N
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1ST. JUDE MEDICAL, INC.
Manufacturer Street387 TECHNOLOGY CIRCLE NW SUITE 500
Manufacturer CityATLANTA GA 30313
Manufacturer CountryUS
Manufacturer Postal Code30313
Single Use3
Previous Use Code3
Removal Correction Number3004936110-06/01/18-001R
Event Type3
Type of Report3

Device Details

Brand NameCARDIOMEMS PATIENT ELECTRONIC SYSTEM
Generic NameSYSTEM, HEMODYNAMIC, IMPLANTABLE
Product CodeMOM
Date Received2020-03-25
Model NumberCM1100
Catalog NumberCM1100
Lot Number6445735
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL, INC.
Manufacturer Address387 TECHNOLOGY CIRCLE NW SUITE 500 ATLANTA GA 30313 US 30313


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-25

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