CADD-SOLIS AMBULATORY INFUSION PUMP 2110 21-2111-0100-51

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 2020-03-04 for CADD-SOLIS AMBULATORY INFUSION PUMP 2110 21-2111-0100-51 manufactured by Smiths Medical Asd, Inc..

Event Text Entries

[182011998] Device evaluation: one smiths medical cadd-solis ambulatory infusion pump was returned for analysis in used condition. Review of the event history log showed the pump displayed an occurrence of a downstream occlusion alarm. Functional testing involved visually inspecting the pump and showed that there was fluid on the downstream occlusion sensor which could cause the pump to have an issue with priming. The investigation determined that fluid ingression was the cause of the reported issue. The downstream occlusion sensor was replaced. Based on evidence and investigation, the complaint allegation was confirmed.
Patient Sequence No: 1, Text Type: N, H10


[182011999] Information was received indicating that a smiths medical cadd-solis ambulatory infusion pump was unable to prime. No adverse effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3012307300-2020-01827
MDR Report Key9788033
Report SourceUSER FACILITY
Date Received2020-03-04
Date of Report2020-03-04
Date Mfgr Received2020-02-17
Device Manufacturer Date2012-04-17
Date Added to Maude2020-03-04
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 Phone3833310
Manufacturer G1SMITHS MEDICAL ASD, INC.
Manufacturer Street3350 GRANADA AVE. N. SUITE 100
Manufacturer CityOAKDALE, MN
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCADD-SOLIS AMBULATORY INFUSION PUMP
Generic NamePUMP, INFUSION, PCA
Product CodeMEA
Date Received2020-03-04
Returned To Mfg2020-02-14
Model Number2110
Catalog Number21-2111-0100-51
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 2020-03-04

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