CADD SOLIS HPCA PUMP 2110 21-2112-0100-51

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-16 for CADD SOLIS HPCA PUMP 2110 21-2112-0100-51 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[183479201] Device evaluation returned device was received in good physical condition. No evidence of reported problem in event log. During the evaluation of the device the customer's reported problem regarding delivery accuracy was able to be duplicated. Three separate delivery accuracy tests were performed; at least one test was outside the pump's delivery accuracy manufacturing specifications. The customer reported condition was confirmed. Problem source is unknown. The device history record was reviewed and showed that this device met all manufacturing specification for product released for distribution. No issues were identified that would have impacted this event.
Patient Sequence No: 1, Text Type: N, H10


[183479202] Information was received that a smiths medical cadd solis hpca pump, did not dispense correct amount of medication while on patient. No adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01960
MDR Report Key9833535
Report SourceUSER FACILITY
Date Received2020-03-16
Date of Report2020-03-13
Date of Event2018-02-26
Date Mfgr Received2020-02-12
Device Manufacturer Date2012-07-26
Date Added to Maude2020-03-16
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 ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Manufacturer G1SMITHS MEDICAL ASD, INC
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCADD SOLIS HPCA PUMP
Generic NamePUMP, INFUSION, PCA PRODUCT CODE: MEA
Product CodeMEA
Date Received2020-03-16
Returned To Mfg2020-02-13
Model Number2110
Catalog Number21-2112-0100-51
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS, MN US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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