TERUMO CDI 100 MONITOR

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2012-09-14 for TERUMO CDI 100 MONITOR manufactured by Terumo Cardiovascular Systems Corp..

Event Text Entries

[2978764] It was reported that during use of the device for a cardiopulmonary bypass procedure, the unit would not hold values and was drifting. The device was not changed out, as the user kept running samples and making adjustments. The surgical procedure was completed successfully, and there were no delays, no blood loss, or no adverse consequences to the pt.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1828100-2012-01167
MDR Report Key2750526
Report Source05,06
Date Received2012-09-14
Date of Report2012-08-21
Date of Event2012-08-17
Date Mfgr Received2012-08-21
Date Added to Maude2013-01-02
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 FDA0
Event Location0
Manufacturer ContactKIPP DURBIN
Manufacturer Street6200 JACKSON RD.
Manufacturer CityANN ARBOR MI 48103
Manufacturer CountryUS
Manufacturer Postal48103
Manufacturer Phone7346634145
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTERUMO CDI 100 MONITOR
Product CodeDTY
Date Received2012-09-14
Model Number100
Catalog Number100
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerTERUMO CARDIOVASCULAR SYSTEMS CORP.
Manufacturer AddressANN ARBOR MI 48103 US 48103


Patients

Patient NumberTreatmentOutcomeDate
10 2012-09-14

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.