PCA 7.01 W/ MEDNET 208370401

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 2019-11-08 for PCA 7.01 W/ MEDNET 208370401 manufactured by Icu Medical Costa Rica Ltd..

Event Text Entries

[167018649] The device is available for investigation. It has not been received.
Patient Sequence No: 1, Text Type: N, H10


[167018650] The event involved a lifecare pca pump that the customer reported the pump overdosed and pushed too much of an unspecified medication to the patient. There was patient involvement, however there was no adverse event and no delay in critical therapy.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9615050-2019-00449
MDR Report Key9297606
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-11-08
Date of Report2019-10-16
Date of Event2019-10-15
Date Mfgr Received2019-10-16
Device Manufacturer Date2016-10-20
Date Added to Maude2019-11-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactCHRISTOPHER ZANONI
Manufacturer Street600 N. FIELD DR.
Manufacturer CityLAKE FOREST IL 60045
Manufacturer CountryUS
Manufacturer Postal60045
Manufacturer Phone2247062300
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePCA 7.01 W/ MEDNET
Generic NamePUMP, INFUSION, PCA
Product CodeMEA
Date Received2019-11-08
Catalog Number208370401
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerICU MEDICAL COSTA RICA LTD.
Manufacturer AddressZONA FRANCA GLOBAL LA AURORA HEREDIA CS


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-08

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